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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HMU2
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.747 |
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 613 | 617 | PF00656 | 0.747 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.636 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 614 | 616 | PF00082 | 0.690 |
CLV_PCSK_PC7_1 | 46 | 52 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.725 |
DEG_APCC_DBOX_1 | 453 | 461 | PF00400 | 0.635 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.473 |
DEG_SPOP_SBC_1 | 394 | 398 | PF00917 | 0.509 |
DEG_SPOP_SBC_1 | 424 | 428 | PF00917 | 0.718 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.504 |
DOC_CYCLIN_RxL_1 | 120 | 130 | PF00134 | 0.500 |
DOC_CYCLIN_RxL_1 | 242 | 254 | PF00134 | 0.302 |
DOC_CYCLIN_RxL_1 | 449 | 461 | PF00134 | 0.637 |
DOC_MAPK_DCC_7 | 306 | 316 | PF00069 | 0.734 |
DOC_MAPK_gen_1 | 139 | 148 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 185 | 192 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 72 | 79 | PF00069 | 0.346 |
DOC_PP1_RVXF_1 | 530 | 537 | PF00149 | 0.630 |
DOC_PP2B_LxvP_1 | 623 | 626 | PF13499 | 0.652 |
DOC_PP2B_LxvP_1 | 644 | 647 | PF13499 | 0.748 |
DOC_PP4_FxxP_1 | 128 | 131 | PF00568 | 0.389 |
DOC_PP4_FxxP_1 | 512 | 515 | PF00568 | 0.626 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.777 |
DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.718 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.521 |
LIG_14-3-3_CanoR_1 | 117 | 127 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 236 | 246 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 289 | 298 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 301 | 308 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 370 | 376 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 446 | 452 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 520 | 528 | PF00244 | 0.753 |
LIG_14-3-3_CanoR_1 | 89 | 99 | PF00244 | 0.574 |
LIG_Actin_WH2_2 | 401 | 419 | PF00022 | 0.487 |
LIG_APCC_ABBAyCdc20_2 | 248 | 254 | PF00400 | 0.416 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.497 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.517 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.487 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.509 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.476 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.576 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.737 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.547 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.476 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.546 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.768 |
LIG_HP1_1 | 108 | 112 | PF01393 | 0.443 |
LIG_IBAR_NPY_1 | 495 | 497 | PF08397 | 0.525 |
LIG_LIR_Apic_2 | 463 | 469 | PF02991 | 0.516 |
LIG_LIR_Apic_2 | 509 | 515 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 167 | 178 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 249 | 260 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 272 | 282 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 640 | 649 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 640 | 644 | PF02991 | 0.498 |
LIG_LYPXL_SIV_4 | 443 | 451 | PF13949 | 0.633 |
LIG_PCNA_yPIPBox_3 | 446 | 460 | PF02747 | 0.540 |
LIG_Pex14_2 | 637 | 641 | PF04695 | 0.508 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.509 |
LIG_SH2_CRK | 541 | 545 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 541 | 545 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 584 | 588 | PF00017 | 0.652 |
LIG_SH2_PTP2 | 503 | 506 | PF00017 | 0.405 |
LIG_SH2_SRC | 459 | 462 | PF00017 | 0.644 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.613 |
LIG_SH2_STAT3 | 497 | 500 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.560 |
LIG_SH3_1 | 527 | 533 | PF00018 | 0.662 |
LIG_SH3_1 | 541 | 547 | PF00018 | 0.566 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.488 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.487 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.545 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.648 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.550 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.722 |
LIG_SUMO_SIM_anti_2 | 209 | 214 | PF11976 | 0.487 |
LIG_SUMO_SIM_anti_2 | 73 | 78 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 223 | 228 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.406 |
LIG_SxIP_EBH_1 | 424 | 436 | PF03271 | 0.721 |
LIG_TRAF2_1 | 364 | 367 | PF00917 | 0.769 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.690 |
LIG_TRAF2_1 | 610 | 613 | PF00917 | 0.482 |
LIG_TRAF2_2 | 318 | 323 | PF00917 | 0.684 |
LIG_TYR_ITIM | 250 | 255 | PF00017 | 0.542 |
LIG_TYR_ITIM | 273 | 278 | PF00017 | 0.501 |
MOD_CDC14_SPxK_1 | 464 | 467 | PF00782 | 0.515 |
MOD_CDK_SPK_2 | 127 | 132 | PF00069 | 0.207 |
MOD_CDK_SPxK_1 | 461 | 467 | PF00069 | 0.522 |
MOD_CDK_SPxxK_3 | 19 | 26 | PF00069 | 0.490 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.538 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.533 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.693 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.614 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.413 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.554 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.532 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.757 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.712 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.740 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.706 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.504 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.406 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.649 |
MOD_GlcNHglycan | 633 | 637 | PF01048 | 0.713 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.532 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.328 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.328 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.559 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.652 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.626 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.481 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.248 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.328 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.484 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.209 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.387 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.536 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.505 |
MOD_NEK2_2 | 269 | 274 | PF00069 | 0.455 |
MOD_PIKK_1 | 301 | 307 | PF00454 | 0.562 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.593 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.753 |
MOD_PKA_1 | 520 | 526 | PF00069 | 0.667 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.621 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.570 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.548 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.765 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.692 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.635 |
MOD_PKB_1 | 42 | 50 | PF00069 | 0.708 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.323 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.666 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.626 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.712 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.516 |
MOD_Plk_2-3 | 288 | 294 | PF00069 | 0.554 |
MOD_Plk_2-3 | 344 | 350 | PF00069 | 0.480 |
MOD_Plk_2-3 | 357 | 363 | PF00069 | 0.694 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.328 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.438 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.714 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.510 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.207 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.638 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.522 |
TRG_DiLeu_BaEn_1 | 494 | 499 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 452 | 457 | PF01217 | 0.630 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.574 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 139 | 144 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 214 | 219 | PF00026 | 0.214 |
TRG_Pf-PMV_PEXEL_1 | 454 | 458 | PF00026 | 0.668 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF63 | Leptomonas seymouri | 70% | 99% |
A0A0S4JFQ6 | Bodo saltans | 45% | 99% |
A0A1X0P5I3 | Trypanosomatidae | 56% | 100% |
A0A3Q8IJ54 | Leishmania donovani | 84% | 100% |
A0A3R7RSH5 | Trypanosoma rangeli | 56% | 100% |
A4IBE4 | Leishmania infantum | 84% | 100% |
C9ZZ76 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AFA0 | Leishmania major | 83% | 100% |
E9B6F5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5C303 | Trypanosoma cruzi | 55% | 96% |