Q0GNC1
Gene name |
Inf2 |
Protein name |
Inverted formin-2 |
Names |
|
Species |
Mus musculus (Mouse) |
KEGG Pathway |
mmu:70435 |
EC number |
|
Protein Class |
|

Descriptions
Autoinhibitory domains (AIDs)
Target domain |
589-1032 (FH2 domain) |
Relief mechanism |
Partner binding |
Assay |
|
Target domain |
589-1032 (FH2 domain) |
Relief mechanism |
Partner binding |
Assay |
|
Accessory elements
No accessory elements
References
- Ramabhadran V et al. (2013) "Actin monomers activate inverted formin 2 by competing with its autoinhibitory interaction", The Journal of biological chemistry, 288, 26847-55
- Higashi T et al. (2010) "Flightless-I (Fli-I) regulates the actin assembly activity of diaphanous-related formins (DRFs) Daam1 and mDia1 in cooperation with active Rho GTPase", The Journal of biological chemistry, 285, 16231-8
Autoinhibited structure

Activated structure

1 structures for Q0GNC1
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-Q0GNC1-F1 | Predicted | AlphaFoldDB |
No variants for Q0GNC1
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
No variants for Q0GNC1 |
No associated diseases with Q0GNC1
1 GO annotations of cellular component
Name | Definition |
---|---|
perinuclear region of cytoplasm | Cytoplasm situated near, or occurring around, the nucleus. |
2 GO annotations of molecular function
Name | Definition |
---|---|
actin binding | Binding to monomeric or multimeric forms of actin, including actin filaments. |
small GTPase binding | Binding to a small monomeric GTPase. |
3 GO annotations of biological process
Name | Definition |
---|---|
actin cytoskeleton organization | A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of cytoskeletal structures comprising actin filaments and their associated proteins. |
regulation of cellular component size | A process that modulates the size of a cellular component. |
regulation of mitochondrial fission | Any process that modulates the rate, frequency or extent of mitochondrial fission. Mitochondrial fission is the division of a mitochondrion within a cell to form two or more separate mitochondrial compartments. |
12 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
A0A1D5P556 | DAAM2 | Disheveled-associated activator of morphogenesis 2 | Gallus gallus (Chicken) | SS |
O95466 | FMNL1 | Formin-like protein 1 | Homo sapiens (Human) | SS |
Q9Y4D1 | DAAM1 | Disheveled-associated activator of morphogenesis 1 | Homo sapiens (Human) | EV |
Q86T65 | DAAM2 | Disheveled-associated activator of morphogenesis 2 | Homo sapiens (Human) | SS |
Q27J81 | INF2 | Inverted formin-2 | Homo sapiens (Human) | EV |
Q80U19 | Daam2 | Disheveled-associated activator of morphogenesis 2 | Mus musculus (Mouse) | SS |
Q8BPM0 | Daam1 | Disheveled-associated activator of morphogenesis 1 | Mus musculus (Mouse) | PR |
Q0QWG9 | Grid2ip | Delphilin | Mus musculus (Mouse) | PR |
Q9C7S1 | FH12 | Formin-like protein 12 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9LH02 | FH17 | Formin-like protein 17 | Arabidopsis thaliana (Mouse-ear cress) | PR |
P0C5K4 | FH21A | Putative formin-like protein 21a | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9FF14 | FH19 | Formin-like protein 19 | Arabidopsis thaliana (Mouse-ear cress) | PR |
10 | 20 | 30 | 40 | 50 | 60 |
MSVKEGAQRK | WAALKEKLGP | QDSDPTEANL | ESAEPELCIR | LLQMPSVVNY | SGLRKRLESS |
70 | 80 | 90 | 100 | 110 | 120 |
DGGWMVQFLE | QSGLDLLLEA | LARLSGRGVA | RISDALLQLT | CISCVRAVMN | SQQGIEYILS |
130 | 140 | 150 | 160 | 170 | 180 |
NQGYVRQLSQ | ALDTSNVMVK | KQVFELLAAL | CIYSPEGHAL | TLDALDHYKM | VCSQQYRFSV |
190 | 200 | 210 | 220 | 230 | 240 |
IMSELSDSDN | VPYVVTLLSV | INAIILGPED | LRSRAQLRSE | FIGLQLLDIL | TRLRDLEDAD |
250 | 260 | 270 | 280 | 290 | 300 |
LLIQLEAFEE | AKAEDEEELQ | RISDGINMNS | HQEVFASLFH | KVSCSPASAQ | LLSVLQGLMH |
310 | 320 | 330 | 340 | 350 | 360 |
LEPAGRSGQL | LWEALENLVN | RAVLLASDAQ | ACTLEEVVER | LLSIKGRPRP | SPLDKAHKSV |
370 | 380 | 390 | 400 | 410 | 420 |
QTNSVQNQGS | SSQNTTTPTT | KVEGQQPVVA | SPCQHVGSIQ | SSSVDIAPQP | VALEQCITAL |
430 | 440 | 450 | 460 | 470 | 480 |
PLPTPPLSSS | TPVLPPTPPP | LPGPGATSPL | PPPPPPLPPP | LPGSGTTSPP | PPPPPPPPLP |
490 | 500 | 510 | 520 | 530 | 540 |
PPLPGSGTIS | PPPPPPPPPL | PGTGAVSPPP | PPPLPSLPDS | HKTQPPPPPP | PPLPGMCPVP |
550 | 560 | 570 | 580 | 590 | 600 |
PPPPLPRAGQ | IPPPPPLPGF | SVPSMMGGVE | EIIVAQVDHS | LGSAWVPSHR | RVNPPTLRMK |
610 | 620 | 630 | 640 | 650 | 660 |
KLNWQKLPSN | VARERNSMWA | TLGSPCTAAV | EPDFSSIEQL | FSFPTAKPKE | PSAAPARKEP |
670 | 680 | 690 | 700 | 710 | 720 |
KEVTFLDSKK | SLNLNIFLKQ | FKCSNEEVTS | MIQAGDTSKF | DVEVLKQLLK | LLPEKHEIEN |
730 | 740 | 750 | 760 | 770 | 780 |
LRAFTEERAK | LSNADQFYVL | LLDIPCYPLR | VECMMLCEGT | AIVLDMVRPK | AQLVLTACES |
790 | 800 | 810 | 820 | 830 | 840 |
LLTSQRLPVF | CQLILKIGNF | LNYGSHTGDA | DGFKISTLLK | LTETKSQQSR | VTLLHHVLEE |
850 | 860 | 870 | 880 | 890 | 900 |
VEKSHPDLLQ | LSRDLEPPSQ | AAGINVEIIH | SEASANLKKL | LEAERKVSAS | IPEVQKQYAE |
910 | 920 | 930 | 940 | 950 | 960 |
RLQASIEASQ | ELDKVFDAIE | QKKLELADYL | CEDPQQLSLE | DTFSTMKTFR | DLFTRALKEN |
970 | 980 | 990 | 1000 | 1010 | 1020 |
KDRKEQMAKA | ERRKQQLAEE | EARRPRDEDG | KPIRKGPGKQ | EEVCVIDALL | ADIRKGFQLR |
1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
KTARGRGDTE | ASGRVAPTDP | PKATEPATAS | NPTQGTNHPA | SEPLDTTAAD | EPQGWDLVDA |
1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
VTPSPQPSKE | EDGPPALERR | SSWYVDAIDF | LDPEDTPDAQ | PSEGVWPVTL | GDGQALNPLE |
1150 | 1160 | 1170 | 1180 | 1190 | 1200 |
FSSNKPPGVK | SSHQDATDPE | ALWGVHQTEA | DSTSEGPEDE | AQRGQSTHLP | RTGPGEDEDG |
1210 | 1220 | 1230 | 1240 | 1250 | 1260 |
EDTAPESALD | TSLDRSFSED | AVTDSSGSGT | LPRVQGRVSK | GTSKRRKKRP | SRNQEEFVPD |
1270 | |||||
SDDIKAKRLC | VIQ |