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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005885 | Arp2/3 protein complex | 2 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
Related structures:
AlphaFold database: Q4QDV0
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007015 | actin filament organization | 5 | 7 |
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0030029 | actin filament-based process | 2 | 2 |
GO:0030036 | actin cytoskeleton organization | 3 | 2 |
GO:0030832 | regulation of actin filament length | 5 | 7 |
GO:0030833 | regulation of actin filament polymerization | 7 | 7 |
GO:0032271 | regulation of protein polymerization | 6 | 7 |
GO:0032535 | regulation of cellular component size | 4 | 7 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 7 |
GO:0032970 | regulation of actin filament-based process | 4 | 7 |
GO:0033043 | regulation of organelle organization | 5 | 7 |
GO:0034314 | Arp2/3 complex-mediated actin nucleation | 7 | 7 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 7 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 7 |
GO:0045010 | actin nucleation | 6 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051128 | regulation of cellular component organization | 4 | 7 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065008 | regulation of biological quality | 2 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
GO:0090066 | regulation of anatomical structure size | 3 | 7 |
GO:0097435 | supramolecular fiber organization | 4 | 7 |
GO:0110053 | regulation of actin filament organization | 6 | 7 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 7 |
GO:0005198 | structural molecule activity | 1 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0005515 | protein binding | 2 | 7 |
GO:0008092 | cytoskeletal protein binding | 3 | 7 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
GO:0051015 | actin filament binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.602 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.361 |
DEG_APCC_DBOX_1 | 607 | 615 | PF00400 | 0.654 |
DEG_SCF_TRCP1_1 | 342 | 347 | PF00400 | 0.500 |
DEG_SIAH_1 | 85 | 93 | PF03145 | 0.576 |
DEG_SPOP_SBC_1 | 247 | 251 | PF00917 | 0.564 |
DEG_SPOP_SBC_1 | 79 | 83 | PF00917 | 0.679 |
DOC_CDC14_PxL_1 | 175 | 183 | PF14671 | 0.513 |
DOC_CDC14_PxL_1 | 385 | 393 | PF14671 | 0.593 |
DOC_MAPK_gen_1 | 512 | 521 | PF00069 | 0.628 |
DOC_MAPK_HePTP_8 | 509 | 521 | PF00069 | 0.646 |
DOC_MAPK_MEF2A_6 | 176 | 183 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 512 | 521 | PF00069 | 0.628 |
DOC_PP1_RVXF_1 | 378 | 385 | PF00149 | 0.368 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.608 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 234 | 239 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 252 | 257 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 297 | 304 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 380 | 385 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 426 | 431 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 470 | 474 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 477 | 486 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 540 | 546 | PF00244 | 0.791 |
LIG_14-3-3_CanoR_1 | 565 | 573 | PF00244 | 0.787 |
LIG_14-3-3_CanoR_1 | 615 | 620 | PF00244 | 0.659 |
LIG_CSL_BTD_1 | 133 | 136 | PF09270 | 0.574 |
LIG_CSL_BTD_1 | 328 | 331 | PF09270 | 0.567 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.555 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.572 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.601 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.465 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.630 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.669 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.834 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.574 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.766 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.580 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.667 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 429 | 433 | PF02991 | 0.497 |
LIG_MYND_1 | 21 | 25 | PF01753 | 0.739 |
LIG_REV1ctd_RIR_1 | 519 | 528 | PF16727 | 0.630 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.477 |
LIG_SH3_1 | 623 | 629 | PF00018 | 0.829 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.575 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.674 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.584 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.655 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.825 |
LIG_SH3_4 | 421 | 428 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 575 | 582 | PF11976 | 0.742 |
LIG_SUMO_SIM_par_1 | 180 | 187 | PF11976 | 0.484 |
LIG_UBA3_1 | 580 | 589 | PF00899 | 0.765 |
MOD_CDK_SPK_2 | 416 | 421 | PF00069 | 0.498 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.615 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.583 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.658 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.659 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.699 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.772 |
MOD_Cter_Amidation | 586 | 589 | PF01082 | 0.563 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.427 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.699 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.625 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.608 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.489 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.572 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.739 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.459 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.407 |
MOD_GlcNHglycan | 366 | 371 | PF01048 | 0.734 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.656 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.648 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.605 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.602 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.678 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.527 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.770 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.571 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.553 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.575 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.794 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.659 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.619 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.776 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.650 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.730 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.532 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.745 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.723 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.525 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.473 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.536 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.663 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.707 |
MOD_PIKK_1 | 498 | 504 | PF00454 | 0.745 |
MOD_PK_1 | 252 | 258 | PF00069 | 0.587 |
MOD_PKA_1 | 234 | 240 | PF00069 | 0.636 |
MOD_PKA_1 | 450 | 456 | PF00069 | 0.696 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.734 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.559 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.716 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.692 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.683 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.718 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.654 |
MOD_PKB_1 | 613 | 621 | PF00069 | 0.658 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.510 |
MOD_Plk_1 | 596 | 602 | PF00069 | 0.599 |
MOD_Plk_2-3 | 394 | 400 | PF00069 | 0.588 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.636 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.525 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.599 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.527 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.649 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.719 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.447 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.698 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.508 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.566 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 225 | 230 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 386 | 391 | PF01217 | 0.604 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 612 | 615 | PF00400 | 0.753 |
TRG_Pf-PMV_PEXEL_1 | 228 | 232 | PF00026 | 0.615 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8H8 | Leptomonas seymouri | 37% | 100% |
A0A3Q8IA03 | Leishmania donovani | 89% | 100% |
A4H9K0 | Leishmania braziliensis | 70% | 100% |
A4HXW5 | Leishmania infantum | 89% | 100% |
E9ARM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |