Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 1 |
NetGPI | no | yes: 0, no: 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005885 | Arp2/3 protein complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H473
Term | Name | Level | Count |
---|---|---|---|
GO:0007015 | actin filament organization | 5 | 2 |
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0030832 | regulation of actin filament length | 5 | 2 |
GO:0030833 | regulation of actin filament polymerization | 7 | 2 |
GO:0032271 | regulation of protein polymerization | 6 | 2 |
GO:0032535 | regulation of cellular component size | 4 | 2 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 2 |
GO:0032970 | regulation of actin filament-based process | 4 | 2 |
GO:0033043 | regulation of organelle organization | 5 | 2 |
GO:0034314 | Arp2/3 complex-mediated actin nucleation | 7 | 2 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 2 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 2 |
GO:0045010 | actin nucleation | 6 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051128 | regulation of cellular component organization | 4 | 2 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090066 | regulation of anatomical structure size | 3 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
GO:0110053 | regulation of actin filament organization | 6 | 2 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.610 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.828 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.828 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.721 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.599 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.839 |
DOC_CYCLIN_RxL_1 | 141 | 151 | PF00134 | 0.603 |
DOC_CYCLIN_RxL_1 | 43 | 50 | PF00134 | 0.716 |
DOC_PP1_RVXF_1 | 44 | 50 | PF00149 | 0.718 |
DOC_PP2B_LxvP_1 | 205 | 208 | PF13499 | 0.650 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.650 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.835 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.804 |
LIG_14-3-3_CanoR_1 | 46 | 52 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 91 | 95 | PF00244 | 0.807 |
LIG_14-3-3_CterR_2 | 276 | 281 | PF00244 | 0.650 |
LIG_BIR_III_4 | 267 | 271 | PF00653 | 0.650 |
LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.725 |
LIG_BRCT_BRCA1_1 | 93 | 97 | PF00533 | 0.795 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.636 |
LIG_GBD_Chelix_1 | 118 | 126 | PF00786 | 0.602 |
LIG_LIR_Apic_2 | 89 | 95 | PF02991 | 0.813 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.724 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.792 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.718 |
LIG_Pex14_2 | 97 | 101 | PF04695 | 0.789 |
LIG_REV1ctd_RIR_1 | 42 | 50 | PF16727 | 0.719 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.801 |
LIG_SH2_NCK_1 | 92 | 96 | PF00017 | 0.801 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.650 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.688 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.650 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.650 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.650 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.711 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.805 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.486 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.650 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.846 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.805 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.846 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.816 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.643 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.518 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.449 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.738 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.576 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.639 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.783 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.499 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.779 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.585 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.366 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.840 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.818 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.804 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.800 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.603 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.434 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.648 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.784 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.362 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.723 |
MOD_PK_1 | 135 | 141 | PF00069 | 0.630 |
MOD_PK_1 | 196 | 202 | PF00069 | 0.601 |
MOD_PKA_1 | 90 | 96 | PF00069 | 0.808 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.808 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.636 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.636 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.661 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.726 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.462 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.650 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.832 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.748 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.804 |
MOD_SUMO_for_1 | 77 | 80 | PF00179 | 0.849 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.712 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.650 |
TRG_ER_diArg_1 | 143 | 145 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.617 |
TRG_NES_CRM1_1 | 127 | 141 | PF08389 | 0.629 |