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

3 structures for P97457

Entry ID Method Resolution Chain Position Source
7NEP EM 1020 A R/S 21-164 PDB
7QIO EM 900 A P/Q 1-169 PDB
AF-P97457-F1 Predicted AlphaFoldDB

11 variants for P97457

Variant ID(s) Position Change Description Diseaes Association Provenance
rs3388953029 2 A>T No EVA
rs3388949109 23 D>Y No EVA
rs3388948887 25 T>I No EVA
rs3413085472 48 E>G No EVA
rs3388922300 56 A>G No EVA
rs3398543687 82 V>G No EVA
rs3398538659 85 T>I No EVA
rs3398471698 90 K>T No EVA
rs13472362 129 D>G No EVA
rs3388952429 131 F>I No EVA
rs3388953180 150 N>K No EVA

No associated diseases with P97457

3 regional properties for P97457

Type Name Position InterPro Accession
domain EF-hand domain 25 - 60 IPR002048-1
domain EF-hand domain 95 - 130 IPR002048-2
binding_site EF-Hand 1, calcium-binding site 38 - 50 IPR018247

Functions

Description
EC Number
Subcellular Localization
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

2 GO annotations of cellular component

Name Definition
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
myosin complex A protein complex, formed of one or more myosin heavy chains plus associated light chains and other proteins, that functions as a molecular motor; uses the energy of ATP hydrolysis to move actin filaments or to move vesicles or other cargo on fixed actin filaments; has magnesium-ATPase activity and binds actin. Myosin classes are distinguished based on sequence features of the motor, or head, domain, but also have distinct tail regions that are believed to bind specific cargoes.

2 GO annotations of molecular function

Name Definition
calcium ion binding Binding to a calcium ion (Ca2+).
structural constituent of muscle The action of a molecule that contributes to the structural integrity of a muscle fiber.

3 GO annotations of biological process

Name Definition
immune response Any immune system process that functions in the calibrated response of an organism to a potential internal or invasive threat.
muscle contraction A process in which force is generated within muscle tissue, resulting in a change in muscle geometry. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis.
skeletal muscle tissue development The developmental sequence of events leading to the formation of adult skeletal muscle tissue. The main events are: the fusion of myoblasts to form myotubes that increase in size by further fusion to them of myoblasts, the formation of myofibrils within their cytoplasm and the establishment of functional neuromuscular junctions with motor neurons. At this stage they can be regarded as mature muscle fibers.

9 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q5E9E2 MYL9 Myosin regulatory light polypeptide 9 Bos taurus (Bovine) PR
P19105 MYL12A Myosin regulatory light chain 12A Homo sapiens (Human) PR
Q9BUA6 MYL10 Myosin regulatory light chain 10 Homo sapiens (Human) PR
O14950 MYL12B Myosin regulatory light chain 12B Homo sapiens (Human) PR
P51667 Myl2 Myosin regulatory light chain 2, ventricular/cardiac muscle isoform Mus musculus (Mouse) PR
Q3THE2 Myl12b Myosin regulatory light chain 12B Mus musculus (Mouse) PR
Q62082 Myl10 Myosin regulatory light chain 10 Mus musculus (Mouse) PR
P13832 Rlc-a Myosin regulatory light chain RLC-A Rattus norvegicus (Rat) PR
P18666 Myl12b Myosin regulatory light chain 12B Rattus norvegicus (Rat) PR
10 20 30 40 50 60
MAPKKAKRRA GAEGSSNVFS MFDQTQIQEF KEAFTVIDQN RDGIIDKEDL RDTFAAMGRL
70 80 90 100 110 120
NVKNEELDAM MKEASGPINF TVFLTMFGEK LKGADPEDVI TGAFKVLDPE GKGTIKKQFL
130 140 150 160
EELLTTQCDR FSQEEIKNMW AAFPPDVGGN VDYKNICYVI THGDAKDQE