Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

1 structures for Q9LZD4

Entry ID Method Resolution Chain Position Source
AF-Q9LZD4-F1 Predicted AlphaFoldDB

2 variants for Q9LZD4

Variant ID(s) Position Change Description Diseaes Association Provenance
ENSVATH06916035 202 A>P No 1000Genomes
ENSVATH06916035 202 A>S No 1000Genomes

1 associated diseases with Q9LZD4

[MIM: 182601]: Spastic paraplegia 4, autosomal dominant (SPG4)

A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. {ECO:0000269|PubMed:10610178, ECO:0000269|PubMed:10699187, ECO:0000269|PubMed:11015453, ECO:0000269|PubMed:11039577, ECO:0000269|PubMed:11087788, ECO:0000269|PubMed:11309678, ECO:0000269|PubMed:11809724, ECO:0000269|PubMed:11843700, ECO:0000269|PubMed:11985387, ECO:0000269|PubMed:12124993, ECO:0000269|PubMed:12161613, ECO:0000269|PubMed:12163196, ECO:0000269|PubMed:12202986, ECO:0000269|PubMed:12460147, ECO:0000269|PubMed:12552568, ECO:0000269|PubMed:12939659, ECO:0000269|PubMed:14732620, ECO:0000269|PubMed:15159500, ECO:0000269|PubMed:15210521, ECO:0000269|PubMed:15248095, ECO:0000269|PubMed:15326248, ECO:0000269|PubMed:15482961, ECO:0000269|PubMed:15667412, ECO:0000269|PubMed:15716377, ECO:0000269|PubMed:15891913, ECO:0000269|PubMed:16339213, ECO:0000269|PubMed:16682546, ECO:0000269|PubMed:16684598, ECO:0000269|PubMed:17389232, ECO:0000269|PubMed:17594340, ECO:0000269|PubMed:19000169, ECO:0000269|PubMed:20214791, ECO:0000269|PubMed:20550563, ECO:0000269|PubMed:20562464, ECO:0000269|PubMed:20718791, ECO:0000269|PubMed:20932283, ECO:0000269|PubMed:21546041, ECO:0000269|PubMed:22960362, ECO:0000269|PubMed:23279441, ECO:0000269|PubMed:24824479, ECO:0000269|PubMed:25045380, ECO:0000269|PubMed:25421405, ECO:0000269|PubMed:28572275}. Note=The disease is caused by variants affecting the gene represented in this entry.

Without disease ID
  • A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. {ECO:0000269|PubMed:10610178, ECO:0000269|PubMed:10699187, ECO:0000269|PubMed:11015453, ECO:0000269|PubMed:11039577, ECO:0000269|PubMed:11087788, ECO:0000269|PubMed:11309678, ECO:0000269|PubMed:11809724, ECO:0000269|PubMed:11843700, ECO:0000269|PubMed:11985387, ECO:0000269|PubMed:12124993, ECO:0000269|PubMed:12161613, ECO:0000269|PubMed:12163196, ECO:0000269|PubMed:12202986, ECO:0000269|PubMed:12460147, ECO:0000269|PubMed:12552568, ECO:0000269|PubMed:12939659, ECO:0000269|PubMed:14732620, ECO:0000269|PubMed:15159500, ECO:0000269|PubMed:15210521, ECO:0000269|PubMed:15248095, ECO:0000269|PubMed:15326248, ECO:0000269|PubMed:15482961, ECO:0000269|PubMed:15667412, ECO:0000269|PubMed:15716377, ECO:0000269|PubMed:15891913, ECO:0000269|PubMed:16339213, ECO:0000269|PubMed:16682546, ECO:0000269|PubMed:16684598, ECO:0000269|PubMed:17389232, ECO:0000269|PubMed:17594340, ECO:0000269|PubMed:19000169, ECO:0000269|PubMed:20214791, ECO:0000269|PubMed:20550563, ECO:0000269|PubMed:20562464, ECO:0000269|PubMed:20718791, ECO:0000269|PubMed:20932283, ECO:0000269|PubMed:21546041, ECO:0000269|PubMed:22960362, ECO:0000269|PubMed:23279441, ECO:0000269|PubMed:24824479, ECO:0000269|PubMed:25045380, ECO:0000269|PubMed:25421405, ECO:0000269|PubMed:28572275}. Note=The disease is caused by variants affecting the gene represented in this entry.

4 regional properties for Q9LZD4

Type Name Position InterPro Accession
domain Protein kinase domain 45 - 301 IPR000719
domain AGC-kinase, C-terminal 302 - 354 IPR000961
active_site Serine/threonine-protein kinase, active site 164 - 176 IPR008271
binding_site Protein kinase, ATP binding site 51 - 74 IPR017441

Functions

Description
EC Number
Subcellular Localization
  • Golgi apparatus membrane
  • Cell membrane ; Lipid-anchor
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

3 GO annotations of cellular component

Name Definition
Golgi membrane The lipid bilayer surrounding any of the compartments of the Golgi apparatus.
intracellular membrane-bounded organelle Organized structure of distinctive morphology and function, bounded by a single or double lipid bilayer membrane and occurring within the cell. Includes the nucleus, mitochondria, plastids, vacuoles, and vesicles. Excludes the plasma membrane.
plasma membrane The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.

2 GO annotations of molecular function

Name Definition
GTP binding Binding to GTP, guanosine triphosphate.
GTPase activity Catalysis of the reaction: GTP + H2O = GDP + H+ + phosphate.

3 GO annotations of biological process

Name Definition
protein secretion The controlled release of proteins from a cell.
regulation of exocytosis Any process that modulates the frequency, rate or extent of exocytosis.
vesicle docking involved in exocytosis The initial attachment of a vesicle membrane to a target membrane, mediated by proteins protruding from the membrane of the vesicle and the target membrane, that contributes to exocytosis.

29 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
P07560 SEC4 Ras-related protein SEC4 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) PR
Q1RMR4 RAB15 Ras-related protein Rab-15 Bos taurus (Bovine) PR
Q2HJI8 RAB8B Ras-related protein Rab-8B Bos taurus (Bovine) PR
A4FV54 RAB8A Ras-related protein Rab-8A Bos taurus (Bovine) PR
Q5F470 RAB8A Ras-related protein Rab-8A Gallus gallus (Chicken) PR
P61007 RAB8A Ras-related protein Rab-8A Canis lupus familiaris (Dog) (Canis familiaris) PR
P51152 RAB12 Ras-related protein Rab-12 Canis lupus familiaris (Dog) (Canis familiaris) PR
P0C0E4 RAB40AL Ras-related protein Rab-40A-like Homo sapiens (Human) PR
Q12829 RAB40B Ras-related protein Rab-40B Homo sapiens (Human) PR
Q6IQ22 RAB12 Ras-related protein Rab-12 Homo sapiens (Human) PR
Q8WXH6 RAB40A Ras-related protein Rab-40A Homo sapiens (Human) PR
Q92930 RAB8B Ras-related protein Rab-8B Homo sapiens (Human) PR
Q96S21 RAB40C Ras-related protein Rab-40C Homo sapiens (Human) PR
P61006 RAB8A Ras-related protein Rab-8A Homo sapiens (Human) PR
Q8K386 Rab15 Ras-related protein Rab-15 Mus musculus (Mouse) PR
Q8CB87 Rab44 Ras-related protein Rab-44 Mus musculus (Mouse) PR
P35283 Rab12 Ras-related protein Rab-12 Mus musculus (Mouse) PR
P55258 Rab8a Ras-related protein Rab-8A Mus musculus (Mouse) PR
P61028 Rab8b Ras-related protein Rab-8B Mus musculus (Mouse) PR
Q8VHQ4 Rab40c Ras-related protein Rab-40C Mus musculus (Mouse) PR
Q9DD03 Rab13 Ras-related protein Rab-13 Mus musculus (Mouse) PR
Q8VHP8 Rab40b Ras-related protein Rab-40B Mus musculus (Mouse) PR
P35289 Rab15 Ras-related protein Rab-15 Rattus norvegicus (Rat) PR
P35280 Rab8a Ras-related protein Rab-8A Rattus norvegicus (Rat) PR
P35284 Rab12 Ras-related protein Rab-12 Rattus norvegicus (Rat) PR
P70550 Rab8b Ras-related protein Rab-8B Rattus norvegicus (Rat) PR
P35281 Rab10 Ras-related protein Rab-10 Rattus norvegicus (Rat) PR
O24466 RABE1A Ras-related protein RABE1a Arabidopsis thaliana (Mouse-ear cress) PR
Q9SF91 RABE1E Ras-related protein RABE1e Arabidopsis thaliana (Mouse-ear cress) PR
10 20 30 40 50 60
MAVAPARARS DYDYLIKLLL IGDSGVGKSC LLLRFSDDTF TTSFITTIGI DFKIRTVELD
70 80 90 100 110 120
GKRIKLQIWD TAGQERFRTI TTAYYRGAMG ILLVYDVTDE SSFNNIRNWM KNIEQHASDN
130 140 150 160 170 180
VNKILVGNKA DMDESKRAVP TAKGQALADE YGIKFFETSA KTNLNVENVF MSIAKDIKQR
190 200 210
LTETDTKAEP QGIKITKQDT AASSSTAEKS ACCSYV