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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005885 | Arp2/3 protein complex | 2 | 9 |
GO:0032991 | protein-containing complex | 1 | 9 |
Related structures:
AlphaFold database: A4H9K0
Term | Name | Level | Count |
---|---|---|---|
GO:0007015 | actin filament organization | 5 | 9 |
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016043 | cellular component organization | 3 | 9 |
GO:0030832 | regulation of actin filament length | 5 | 9 |
GO:0030833 | regulation of actin filament polymerization | 7 | 9 |
GO:0032271 | regulation of protein polymerization | 6 | 9 |
GO:0032535 | regulation of cellular component size | 4 | 9 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 9 |
GO:0032970 | regulation of actin filament-based process | 4 | 9 |
GO:0033043 | regulation of organelle organization | 5 | 9 |
GO:0034314 | Arp2/3 complex-mediated actin nucleation | 7 | 9 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 9 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 9 |
GO:0045010 | actin nucleation | 6 | 9 |
GO:0050789 | regulation of biological process | 2 | 9 |
GO:0050794 | regulation of cellular process | 3 | 9 |
GO:0051128 | regulation of cellular component organization | 4 | 9 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 9 |
GO:0065007 | biological regulation | 1 | 9 |
GO:0065008 | regulation of biological quality | 2 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
GO:0090066 | regulation of anatomical structure size | 3 | 9 |
GO:0097435 | supramolecular fiber organization | 4 | 9 |
GO:0110053 | regulation of actin filament organization | 6 | 9 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 9 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0030029 | actin filament-based process | 2 | 1 |
GO:0030036 | actin cytoskeleton organization | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005515 | protein binding | 2 | 9 |
GO:0008092 | cytoskeletal protein binding | 3 | 9 |
GO:0005198 | structural molecule activity | 1 | 1 |
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 | 446 | 450 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 526 | 530 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.543 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.543 |
DEG_SPOP_SBC_1 | 479 | 483 | PF00917 | 0.589 |
DOC_CDC14_PxL_1 | 174 | 182 | PF14671 | 0.468 |
DOC_CDC14_PxL_1 | 384 | 392 | PF14671 | 0.409 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.523 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 474 | 480 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 506 | 512 | PF00244 | 0.573 |
LIG_CaM_IQ_9 | 416 | 432 | PF13499 | 0.393 |
LIG_CSL_BTD_1 | 130 | 133 | PF09270 | 0.432 |
LIG_CSL_BTD_1 | 327 | 330 | PF09270 | 0.358 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.391 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.511 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.408 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.423 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.681 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.799 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.588 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.615 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.444 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.532 |
LIG_Integrin_RGD_1 | 467 | 469 | PF01839 | 0.534 |
LIG_LIR_Apic_2 | 78 | 83 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 171 | 182 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 308 | 318 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 91 | 99 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 428 | 432 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.356 |
LIG_SH2_PTP2 | 312 | 315 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.364 |
LIG_SH3_1 | 558 | 564 | PF00018 | 0.671 |
LIG_SH3_2 | 561 | 566 | PF14604 | 0.547 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.420 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.495 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.613 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.441 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.653 |
LIG_SUMO_SIM_anti_2 | 510 | 517 | PF11976 | 0.587 |
LIG_UBA3_1 | 515 | 524 | PF00899 | 0.598 |
MOD_CDC14_SPxK_1 | 248 | 251 | PF00782 | 0.429 |
MOD_CDK_SPxK_1 | 245 | 251 | PF00069 | 0.441 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.658 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.477 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.472 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.521 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.395 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.598 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.629 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.636 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.637 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.623 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.454 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.525 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.520 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.420 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.602 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.642 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.426 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.364 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.395 |
MOD_GlcNHglycan | 239 | 243 | PF01048 | 0.567 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.513 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.625 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.540 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.399 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.411 |
MOD_GlcNHglycan | 366 | 370 | PF01048 | 0.728 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.455 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.725 |
MOD_GlcNHglycan | 449 | 453 | PF01048 | 0.706 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.617 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.535 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.681 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.545 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.346 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.510 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.433 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.553 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.566 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.554 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.532 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.732 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.607 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.756 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.703 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.730 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.517 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.581 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.654 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.606 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.393 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.389 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.511 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.442 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.542 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.593 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.455 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.560 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.359 |
MOD_PK_1 | 163 | 169 | PF00069 | 0.472 |
MOD_PK_1 | 251 | 257 | PF00069 | 0.433 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.605 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.767 |
MOD_Plk_1 | 531 | 537 | PF00069 | 0.580 |
MOD_Plk_2-3 | 393 | 399 | PF00069 | 0.407 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.486 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.525 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.580 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.620 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.610 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.566 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.353 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.328 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.528 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.687 |
TRG_DiLeu_BaLyEn_6 | 224 | 229 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 385 | 390 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.269 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H8 | Leptomonas seymouri | 40% | 97% |
A0A1X0P764 | Trypanosomatidae | 28% | 100% |
A0A3Q8IA03 | Leishmania donovani | 60% | 91% |
A4HXW5 | Leishmania infantum | 60% | 91% |
C9ZZT7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9ARM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 91% |
Q4QDV0 | Leishmania major | 70% | 100% |