Q5AL52
Gene name |
BNI |
Protein name |
Formin BNI1 |
Names |
|
Species |
Candida albicans (strain SC5314 / ATCC MYA-2876) (Yeast) |
KEGG Pathway |
cal:CAALFM_C112960CA |
EC number |
|
Protein Class |
|

Descriptions
(Annotation from UniProt)
The DAD domain regulates activation via by an autoinhibitory interaction with the GBD/FH3 domain. This autoinhibition is released upon competitive binding of an activated GTPase. The release of DAD allows the FH2 domain to then nucleate and elongate nonbranched actin filaments.
Autoinhibitory domains (AIDs)
Target domain |
111-557 (GBD/FH3 domain) |
Relief mechanism |
Partner binding |
Assay |
|
Accessory elements
No accessory elements
References
Autoinhibited structure

Activated structure

1 structures for Q5AL52
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-Q5AL52-F1 | Predicted | AlphaFoldDB |
No variants for Q5AL52
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
No variants for Q5AL52 |
No associated diseases with Q5AL52
4 regional properties for Q5AL52
Functions
9 GO annotations of cellular component
Name | Definition |
---|---|
cell division site | The eventual plane of cell division (also known as cell cleavage or cytokinesis) in a dividing cell. In Eukaryotes, the cleavage apparatus, composed of septin structures and the actomyosin contractile ring, forms along this plane, and the mitotic, or meiotic, spindle is aligned perpendicular to the division plane. In bacteria, the cell division site is generally located at mid-cell and is the site at which the cytoskeletal structure, the Z-ring, assembles. |
cell septum | A structure composed of peptidoglycan and often chitin in addition to other materials. It usually forms perpendicular to the long axis of a cell or hypha and grows centripetally from the cell wall to the center of the cell and often functions in the compartmentalization of a cell into two daughter cells. |
cellular bud neck | The constriction between the mother cell and daughter cell (bud) in an organism that reproduces by budding. |
cellular bud neck contractile ring | A contractile ring, i.e. a cytoskeletal structure composed of actin filaments and myosin, that forms beneath the plasma membrane at the mother-bud neck in mitotic cells that divide by budding in preparation for completing cytokinesis. An example of this structure is found in Saccharomyces cerevisiae. |
cellular bud tip | The end of a cellular bud distal to the site of attachment to the mother cell. |
hyphal tip | The end, or tip, of a fungal hypha, where polarized growth occurs during hyphal elongation. |
incipient cellular bud site | The portion of the budding yeast plasma membrane where a daughter cell will emerge. The yeast marks this spot with bud-site selection proteins before bud emergence occurs. Actin is polarized to this spot just prior to and during bud emergence. |
mating projection tip | The apex of the mating projection in unicellular fungi exposed to mating pheromone; site of polarized growth. |
spitzenkorper | Structure within the hyphal tip of filamentous fungi that acts as an organizing center for hyphal tip growth; may function to supply vesicles to the elongating tip and/or to organize cytoskeletal microfilaments. |
3 GO annotations of molecular function
Name | Definition |
---|---|
actin binding | Binding to monomeric or multimeric forms of actin, including actin filaments. |
cytoskeletal protein binding | Binding to a protein component of a cytoskeleton (actin, microtubule, or intermediate filament cytoskeleton). |
small GTPase binding | Binding to a small monomeric GTPase. |
16 GO annotations of biological process
Name | Definition |
---|---|
actin cortical patch localization | Any process in which actin cortical patches are transported to, or maintained in, a specific location. An actin cortical patch is a discrete actin-containing structure found just beneath the plasma membrane in fungal cells. |
actin filament bundle assembly | The assembly of actin filament bundles; actin filaments are on the same axis but may be oriented with the same or opposite polarities and may be packed with different levels of tightness. |
barbed-end actin filament capping | The binding of a protein or protein complex to the barbed (or plus) end of an actin filament, thus preventing the addition, exchange or removal of further actin subunits. |
cellular bud site selection | The specification of the site where a daughter cell will form, in organisms that reproduce by budding. An example of this process is found in Saccharomyces cerevisiae. |
cellular response to starvation | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of deprivation of nourishment. |
establishment or maintenance of cell polarity | Any cellular process that results in the specification, formation or maintenance of anisotropic intracellular organization or cell growth patterns. |
filamentous growth | The process in which a multicellular organism, a unicellular organism or a group of unicellular organisms grow in a threadlike, filamentous shape. |
filamentous growth of a population of unicellular organisms | The process in which a group of unicellular organisms grow in a threadlike, filamentous shape. |
filamentous growth of a population of unicellular organisms in response to biotic stimulus | The process in which a group of unicellular organisms grow in a threadlike, filamentous shape in response to a biotic (living) stimulus. |
filamentous growth of a population of unicellular organisms in response to chemical stimulus | The process in which a group of unicellular organisms grow in a threadlike, filamentous shape in response to a chemical stimulus. |
filamentous growth of a population of unicellular organisms in response to starvation | The process in which a group of unicellular organisms grow in a threadlike, filamentous shape in response to deprivation of nourishment. |
Golgi localization | Any process in which the Golgi is transported to, and/or maintained in, a specific location within the cell. |
hyphal growth | Growth of fungi as threadlike, tubular structures that may contain multiple nuclei and may or may not be divided internally by septa, or cross-walls. |
maintenance of cell polarity | The maintenance of established anisotropic intracellular organization or cell growth patterns. |
mitotic actomyosin contractile ring assembly | Any actomyosin contractile ring assembly that is involved in mitotic cytokinesis. |
septum digestion after cytokinesis | The process of physically separating the septal cell wall material by enzymatic digestion, that occurs after daughter cells are separated by cytokinesis. |
No homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
No homologous proteins |
10 | 20 | 30 | 40 | 50 | 60 |
MRRRHKDKHN | TDSVSDMSSN | DSASILSSAS | QNSTHSRRSA | SLQSLHSQSH | QYPQGHNNSS |
70 | 80 | 90 | 100 | 110 | 120 |
HRQASTYSIS | SLSPYDKGAS | LSRKSTNISI | SRPIKTNDSN | VFPIKQSFQL | ERPNSAFEIE |
130 | 140 | 150 | 160 | 170 | 180 |
RMFRELLEKL | NFKSLPPQAT | REMLNYDIDR | KWMMIEQDAR | AEYDRQQRYA | RAQNIFSPEE |
190 | 200 | 210 | 220 | 230 | 240 |
YAKVLMSKQV | STNQLSGLWL | ALRSEPIDWV | RRFVYDCQGD | TLLSVYLTKL | QQEMVSCNIT |
250 | 260 | 270 | 280 | 290 | 300 |
DIEDDIFDKE | VNVLQSLKCL | MNQRLGAERI | KTDVDVFVNA | VSGSLLSPRI | ITRKLATDTL |
310 | 320 | 330 | 340 | 350 | 360 |
TFMISYNGNN | DNGRYHKVLR | ALDSINEKSR | MEFDSPDNYS | PRKLTRKPPQ | PANFKRFELW |
370 | 380 | 390 | 400 | 410 | 420 |
LNVVEKTIDA | RGKFRNSDVG | ASDELKSAYA | GTRGSVITTR | NQLENHLVEY | CIATMLLINV |
430 | 440 | 450 | 460 | 470 | 480 |
IVGNGTDYRV | RIHLRAQFRA | AGLDRIIHKF | LELGNEELDN | MITRHKIDAN | NDEEELKYSA |
490 | 500 | 510 | 520 | 530 | 540 |
NFNNEDNEVD | FNDPVNLVQS | LWQSVKNSDA | EGYFLSAIQH | LFLNQSEKRG | NPEEMNRSLR |
550 | 560 | 570 | 580 | 590 | 600 |
VLDGLIQNIS | SVRTVSEDTA | INVAINKLIS | NMSTDDMYRK | ALEDVKIYRR | IAEEATAERD |
610 | 620 | 630 | 640 | 650 | 660 |
DMSRQLSMGA | DGYINSLLND | VKERDMVISR | FRRINEDMKE | ELEQMKTKYM | QEKQESELEM |
670 | 680 | 690 | 700 | 710 | 720 |
RELLIMLNNS | EIGANAVKKD | GGKTTISIST | SNEELAARLK | KQIHRRRAEY | KLDNRQLGTN |
730 | 740 | 750 | 760 | 770 | 780 |
VEPSSRLRAL | RDQMGDIENM | ARELEMTDFE | TYADPEEEEN | NNDQSPEKSE | IDESRSSQES |
790 | 800 | 810 | 820 | 830 | 840 |
EAEIQSVEED | EEEEEKEVVI | PPLPVPSGPK | RAVRNDDLVR | LDHLRKKLAN | LQSESNDIMK |
850 | 860 | 870 | 880 | 890 | 900 |
YNSSSMFNKQ | KFLAMERLQE | LENNFKDFNI | DFAVSDPEDK | YNFNSNAGSV | DDSIKNKTKE |
910 | 920 | 930 | 940 | 950 | 960 |
VLAEAEQIRE | ELRRQLAAAQ | KIKSPSPKRN | TVLERIENKY | VKGQVKIDAP | DVVSNSPRTQ |
970 | 980 | 990 | 1000 | 1010 | 1020 |
KRAHRSTTLN | AMDPKFLQEL | SLKVGKAEPI | QDANNKNQFG | GPLSSSPEDV | SQKHKTSGDS |
1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
SDKDKVLSSP | ISSNDIKSPE | TGNSTTSSAA | PPPPPPPPPP | PPPPLPPILG | GNNSSAAPPP |
1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
PPPPPPPPAF | LNGSGSVIPP | APPLPPPSSG | RSSRSVPSTV | TKSSGSAFDK | IPRPKKKLKQ |
1150 | 1160 | 1170 | 1180 | 1190 | 1200 |
LHWEKIDHSQ | VGNSFWNDPN | THTLVDDLMS | KGIFDEIELI | FAAKEAKKLA | TKKKEDLDKV |
1210 | 1220 | 1230 | 1240 | 1250 | 1260 |
TFLARDISQQ | FSINLHAFNS | FSDEEFVLKV | LRCDKDVLTN | PAVLDFFGKE | DIVEITNTLA |
1270 | 1280 | 1290 | 1300 | 1310 | 1320 |
RNFEPYSTDY | KTEEITKPEK | DPNELQRPDR | IYLELMYNLQ | HYWKSRTRAL | NVVVNYDKDY |
1330 | 1340 | 1350 | 1360 | 1370 | 1380 |
VEYVKKLRLI | DEAVDSIKNS | KHLKGVFEII | LAVGNYMNDS | AKQAHGFKLS | SLQRLSFMKD |
1390 | 1400 | 1410 | 1420 | 1430 | 1440 |
EKNSMTFLHY | VEKVIRTQYP | EFLEFINELS | CCNEITKFSI | ENINNDCKEY | ARAIKNVQSS |
1450 | 1460 | 1470 | 1480 | 1490 | 1500 |
IDIGNLSDVS | KFHPSDRVLK | AVLPALPRAK | RKAELLLDQA | NYTMKEFDDL | MKYFGEDPTD |
1510 | 1520 | 1530 | 1540 | 1550 | 1560 |
QFVKNSFISK | FTDFMKDFKR | VQAENIKREE | ELRVYEQRKK | LLEKPKSSNN | GDSNASDQDG |
1570 | 1580 | 1590 | 1600 | 1610 | 1620 |
ESNEGDGGVM | DSLLQRLKAA | APTKGESASA | RKKALMRKQI | LESQRKRTTG | SVGSPTNVSP |
1630 | 1640 | 1650 | 1660 | 1670 | 1680 |
TRNNESDSGV | DNKDDTHGSS | PLDEQFHDSI | TTQEDRIRDD | NRPPEGVADF | SNVEDPENPD |
1690 | 1700 | 1710 | 1720 | 1730 | |
VGARAKNLLQ | ELRGADESSS | KLSDAQRYRQ | ERLKKKSVQI | DLDEVAKNNN | SE |