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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QAD0
Term | Name | Level | Count |
---|---|---|---|
GO:0000993 | RNA polymerase II complex binding | 5 | 11 |
GO:0001098 | basal transcription machinery binding | 3 | 11 |
GO:0001099 | basal RNA polymerase II transcription machinery binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0008174 | mRNA methyltransferase activity | 5 | 11 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 11 |
GO:0016422 | mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity | 6 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0019899 | enzyme binding | 3 | 11 |
GO:0043175 | RNA polymerase core enzyme binding | 5 | 11 |
GO:0070063 | RNA polymerase binding | 4 | 11 |
GO:0099122 | RNA polymerase II C-terminal domain binding | 6 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 352 | 356 | PF00656 | 0.460 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.727 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.550 |
CLV_PCSK_FUR_1 | 204 | 208 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.391 |
DEG_APCC_DBOX_1 | 33 | 41 | PF00400 | 0.505 |
DEG_COP1_1 | 579 | 587 | PF00400 | 0.494 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.626 |
DOC_CKS1_1 | 214 | 219 | PF01111 | 0.610 |
DOC_CKS1_1 | 339 | 344 | PF01111 | 0.363 |
DOC_MAPK_gen_1 | 287 | 297 | PF00069 | 0.246 |
DOC_MAPK_JIP1_4 | 402 | 408 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 243 | 250 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 402 | 410 | PF00069 | 0.395 |
DOC_PP1_RVXF_1 | 45 | 52 | PF00149 | 0.568 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.395 |
DOC_PP2B_LxvP_1 | 446 | 449 | PF13499 | 0.382 |
DOC_PP4_FxxP_1 | 463 | 466 | PF00568 | 0.536 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.570 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 290 | 296 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 348 | 358 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 390 | 399 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 501 | 507 | PF00244 | 0.524 |
LIG_Clathr_ClatBox_1 | 405 | 409 | PF01394 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 529 | 538 | PF00928 | 0.406 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.335 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.335 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.388 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.403 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.471 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.423 |
LIG_LIR_Apic_2 | 498 | 503 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 579 | 585 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 249 | 260 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 418 | 428 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 443 | 450 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 529 | 539 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 443 | 447 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 529 | 534 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.541 |
LIG_PCNA_yPIPBox_3 | 55 | 69 | PF02747 | 0.415 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.335 |
LIG_Pex14_2 | 534 | 538 | PF04695 | 0.360 |
LIG_SH2_CRK | 500 | 504 | PF00017 | 0.492 |
LIG_SH2_CRK | 582 | 586 | PF00017 | 0.599 |
LIG_SH2_NCK_1 | 114 | 118 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 582 | 586 | PF00017 | 0.511 |
LIG_SH2_PTP2 | 444 | 447 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 392 | 396 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 144 | 147 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.378 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.451 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.315 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.553 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.561 |
LIG_SUMO_SIM_anti_2 | 22 | 27 | PF11976 | 0.514 |
LIG_SUMO_SIM_anti_2 | 443 | 449 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 402 | 407 | PF11976 | 0.393 |
LIG_TYR_ITIM | 442 | 447 | PF00017 | 0.425 |
LIG_WRC_WIRS_1 | 578 | 583 | PF05994 | 0.481 |
MOD_CDK_SPxxK_3 | 568 | 575 | PF00069 | 0.608 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.525 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.534 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.306 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.335 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.530 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.740 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.660 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.608 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.583 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.419 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.468 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.581 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.781 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.563 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.653 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.246 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.335 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.335 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.580 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.644 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.697 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.689 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.679 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.702 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.574 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.293 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.727 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.626 |
MOD_NEK2_2 | 577 | 582 | PF00069 | 0.568 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.246 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.437 |
MOD_PK_1 | 150 | 156 | PF00069 | 0.490 |
MOD_PKA_1 | 2 | 8 | PF00069 | 0.734 |
MOD_PKA_1 | 290 | 296 | PF00069 | 0.246 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.734 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.346 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.424 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.550 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.473 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.614 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.384 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.461 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.505 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.307 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.335 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.335 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.748 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.617 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.610 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.739 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.678 |
MOD_SUMO_rev_2 | 394 | 404 | PF00179 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 400 | 405 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.547 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II31 | Leptomonas seymouri | 63% | 99% |
A0A1X0NXA7 | Trypanosomatidae | 45% | 100% |
A0A3Q8IBG9 | Leishmania donovani | 94% | 100% |
A0A422NWV1 | Trypanosoma rangeli | 47% | 100% |
A4HDR2 | Leishmania braziliensis | 84% | 100% |
A4I108 | Leishmania infantum | 94% | 100% |
C9ZWA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AX46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BAG8 | Trypanosoma cruzi | 46% | 100% |