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:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WWA9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0016192 | vesicle-mediated transport | 4 | 7 |
GO:0043085 | positive regulation of catalytic activity | 4 | 7 |
GO:0043087 | regulation of GTPase activity | 5 | 7 |
GO:0043547 | positive regulation of GTPase activity | 6 | 7 |
GO:0044093 | positive regulation of molecular function | 3 | 7 |
GO:0050790 | regulation of catalytic activity | 3 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
GO:0051336 | regulation of hydrolase activity | 4 | 7 |
GO:0051345 | positive regulation of hydrolase activity | 5 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065009 | regulation of molecular function | 2 | 7 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 7 |
GO:0008047 | enzyme activator activity | 3 | 7 |
GO:0030234 | enzyme regulator activity | 2 | 7 |
GO:0030695 | GTPase regulator activity | 4 | 7 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 7 |
GO:0098772 | molecular function regulator activity | 1 | 7 |
GO:0140677 | molecular function activator activity | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.742 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.587 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.337 |
CLV_PCSK_FUR_1 | 359 | 363 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 536 | 538 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.409 |
CLV_PCSK_PC7_1 | 301 | 307 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.369 |
CLV_Separin_Metazoa | 192 | 196 | PF03568 | 0.738 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.689 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.588 |
DEG_SPOP_SBC_1 | 19 | 23 | PF00917 | 0.644 |
DOC_ANK_TNKS_1 | 71 | 78 | PF00023 | 0.506 |
DOC_CYCLIN_RxL_1 | 309 | 321 | PF00134 | 0.474 |
DOC_CYCLIN_RxL_1 | 567 | 578 | PF00134 | 0.613 |
DOC_MAPK_gen_1 | 305 | 315 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 306 | 315 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 462 | 469 | PF00069 | 0.618 |
DOC_PP1_RVXF_1 | 215 | 222 | PF00149 | 0.662 |
DOC_PP1_RVXF_1 | 571 | 578 | PF00149 | 0.474 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.764 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.695 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.692 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.436 |
LIG_14-3-3_CanoR_1 | 164 | 169 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 226 | 236 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 362 | 368 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 520 | 524 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 78 | 87 | PF00244 | 0.591 |
LIG_APCC_ABBA_1 | 339 | 344 | PF00400 | 0.474 |
LIG_EH1_1 | 375 | 383 | PF00400 | 0.499 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.780 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.499 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.332 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.499 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.543 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.505 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.691 |
LIG_LIR_Apic_2 | 270 | 275 | PF02991 | 0.642 |
LIG_LIR_Apic_2 | 561 | 565 | PF02991 | 0.634 |
LIG_LIR_Gen_1 | 343 | 351 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 452 | 461 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 513 | 523 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 394 | 398 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 428 | 432 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 513 | 518 | PF02991 | 0.551 |
LIG_MYND_1 | 189 | 193 | PF01753 | 0.743 |
LIG_NRBOX | 312 | 318 | PF00104 | 0.474 |
LIG_NRBOX | 504 | 510 | PF00104 | 0.528 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.427 |
LIG_Rb_LxCxE_1 | 27 | 46 | PF01857 | 0.573 |
LIG_Rb_pABgroove_1 | 421 | 429 | PF01858 | 0.474 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.474 |
LIG_SH2_CRK | 486 | 490 | PF00017 | 0.514 |
LIG_SH2_CRK | 515 | 519 | PF00017 | 0.553 |
LIG_SH2_GRB2like | 47 | 50 | PF00017 | 0.650 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 376 | 380 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.566 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.793 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.660 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.693 |
LIG_SUMO_SIM_anti_2 | 475 | 483 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 346 | 353 | PF11976 | 0.474 |
LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.574 |
LIG_TRFH_1 | 337 | 341 | PF08558 | 0.310 |
LIG_UBA3_1 | 454 | 462 | PF00899 | 0.378 |
LIG_WRC_WIRS_1 | 121 | 126 | PF05994 | 0.616 |
LIG_WW_3 | 192 | 196 | PF00397 | 0.692 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.676 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.663 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.643 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.677 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.383 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.345 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.293 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.660 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.631 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.340 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.284 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.326 |
MOD_Cter_Amidation | 76 | 79 | PF01082 | 0.389 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.777 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.647 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.608 |
MOD_GlcNHglycan | 153 | 157 | PF01048 | 0.702 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.598 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.310 |
MOD_GlcNHglycan | 433 | 439 | PF01048 | 0.370 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.506 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.576 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.685 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.611 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.605 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.586 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.389 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.671 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.395 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.276 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.645 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.390 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.469 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.585 |
MOD_LATS_1 | 110 | 116 | PF00433 | 0.590 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.623 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.662 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.499 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.639 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.580 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.340 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.310 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.670 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.418 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.400 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.313 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.634 |
MOD_NEK2_2 | 179 | 184 | PF00069 | 0.579 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.568 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.299 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.310 |
MOD_PKA_1 | 79 | 85 | PF00069 | 0.480 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.661 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.376 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.291 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.478 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.480 |
MOD_PKB_1 | 185 | 193 | PF00069 | 0.640 |
MOD_PKB_1 | 225 | 233 | PF00069 | 0.576 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.709 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.310 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.495 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.576 |
MOD_Plk_2-3 | 347 | 353 | PF00069 | 0.310 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.558 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.501 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.296 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.370 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.621 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.558 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.661 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.310 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.258 |
MOD_SUMO_for_1 | 461 | 464 | PF00179 | 0.399 |
MOD_SUMO_for_1 | 566 | 569 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 212 | 219 | PF00179 | 0.554 |
TRG_DiLeu_BaEn_2 | 525 | 531 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_4 | 526 | 532 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 571 | 573 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.486 |
TRG_NES_CRM1_1 | 421 | 435 | PF08389 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 38 | 42 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P406 | Leptomonas seymouri | 55% | 100% |
A4HYZ3 | Leishmania infantum | 99% | 100% |
E9AIL1 | Leishmania braziliensis | 75% | 100% |
E9AUU4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QCN9 | Leishmania major | 93% | 100% |