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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0030864 | cortical actin cytoskeleton | 7 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HII8
Term | Name | Level | Count |
---|---|---|---|
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0030832 | regulation of actin filament length | 5 | 1 |
GO:0030833 | regulation of actin filament polymerization | 7 | 1 |
GO:0032271 | regulation of protein polymerization | 6 | 1 |
GO:0032535 | regulation of cellular component size | 4 | 1 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 1 |
GO:0032970 | regulation of actin filament-based process | 4 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 1 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090066 | regulation of anatomical structure size | 3 | 1 |
GO:0110053 | regulation of actin filament organization | 6 | 1 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0008092 | cytoskeletal protein binding | 3 | 10 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0051015 | actin filament binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.400 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.298 |
CLV_PCSK_FUR_1 | 145 | 149 | PF00082 | 0.618 |
CLV_PCSK_FUR_1 | 246 | 250 | PF00082 | 0.248 |
CLV_PCSK_FUR_1 | 350 | 354 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.298 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.415 |
DOC_CKS1_1 | 307 | 312 | PF01111 | 0.519 |
DOC_MAPK_gen_1 | 244 | 253 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 352 | 361 | PF00069 | 0.671 |
DOC_MAPK_gen_1 | 41 | 48 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.660 |
DOC_MAPK_RevD_3 | 233 | 249 | PF00069 | 0.503 |
DOC_PP1_RVXF_1 | 235 | 241 | PF00149 | 0.497 |
DOC_PP1_RVXF_1 | 246 | 253 | PF00149 | 0.433 |
DOC_PP4_FxxP_1 | 307 | 310 | PF00568 | 0.496 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.638 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.687 |
LIG_14-3-3_CanoR_1 | 147 | 152 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 185 | 191 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 237 | 245 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 265 | 273 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 334 | 338 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 350 | 360 | PF00244 | 0.561 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.499 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.456 |
LIG_CtBP_PxDLS_1 | 176 | 180 | PF00389 | 0.397 |
LIG_deltaCOP1_diTrp_1 | 228 | 236 | PF00928 | 0.491 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.463 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.392 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.657 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.391 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.488 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.599 |
LIG_LIR_Apic_2 | 305 | 310 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 88 | 98 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.496 |
LIG_LYPXL_S_1 | 271 | 275 | PF13949 | 0.331 |
LIG_LYPXL_yS_3 | 272 | 275 | PF13949 | 0.531 |
LIG_Pex14_2 | 236 | 240 | PF04695 | 0.531 |
LIG_SH2_PTP2 | 50 | 53 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 214 | 217 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.378 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.701 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.735 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.708 |
LIG_SUMO_SIM_anti_2 | 391 | 397 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 175 | 181 | PF11976 | 0.553 |
LIG_TRAF2_1 | 346 | 349 | PF00917 | 0.512 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.493 |
LIG_UBA3_1 | 219 | 224 | PF00899 | 0.476 |
MOD_CDK_SPxxK_3 | 306 | 313 | PF00069 | 0.515 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.660 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.596 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.665 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.665 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.670 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.595 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.704 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.475 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.362 |
MOD_DYRK1A_RPxSP_1 | 172 | 176 | PF00069 | 0.643 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.469 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.532 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.484 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.606 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.535 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.464 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.505 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.758 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.526 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.453 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.443 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.508 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.285 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.505 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.387 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.519 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.598 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.631 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.579 |
MOD_NEK2_2 | 36 | 41 | PF00069 | 0.479 |
MOD_PKA_1 | 147 | 153 | PF00069 | 0.652 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.296 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.643 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.443 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.485 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.685 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.438 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.627 |
MOD_PKB_1 | 145 | 153 | PF00069 | 0.640 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.506 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.630 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.484 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.525 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.616 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.555 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.504 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.684 |
MOD_SUMO_for_1 | 165 | 168 | PF00179 | 0.681 |
MOD_SUMO_rev_2 | 120 | 129 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 19 | 26 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 241 | 245 | PF00179 | 0.418 |
TRG_DiLeu_BaEn_1 | 391 | 396 | PF01217 | 0.377 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5G8 | Leptomonas seymouri | 66% | 100% |
A0A1X0P342 | Trypanosomatidae | 40% | 100% |
A0A3Q8IFZ1 | Leishmania donovani | 84% | 100% |
A4I5T2 | Leishmania infantum | 84% | 100% |
C9ZR53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 92% |
E9B127 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q738 | Leishmania major | 82% | 100% |
V5BMX2 | Trypanosoma cruzi | 43% | 100% |