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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q0K8
Term | Name | Level | Count |
---|---|---|---|
GO:0000993 | RNA polymerase II complex binding | 5 | 8 |
GO:0001098 | basal transcription machinery binding | 3 | 8 |
GO:0001099 | basal RNA polymerase II transcription machinery binding | 4 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005515 | protein binding | 2 | 8 |
GO:0008168 | methyltransferase activity | 4 | 8 |
GO:0008173 | RNA methyltransferase activity | 4 | 8 |
GO:0008174 | mRNA methyltransferase activity | 5 | 8 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 8 |
GO:0016422 | mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity | 6 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 8 |
GO:0019899 | enzyme binding | 3 | 8 |
GO:0043175 | RNA polymerase core enzyme binding | 5 | 8 |
GO:0070063 | RNA polymerase binding | 4 | 8 |
GO:0099122 | RNA polymerase II C-terminal domain binding | 6 | 8 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.518 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 588 | 590 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.376 |
CLV_Separin_Metazoa | 7 | 11 | PF03568 | 0.336 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.464 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.495 |
DEG_SPOP_SBC_1 | 519 | 523 | PF00917 | 0.328 |
DOC_CKS1_1 | 146 | 151 | PF01111 | 0.495 |
DOC_CKS1_1 | 295 | 300 | PF01111 | 0.490 |
DOC_CYCLIN_RxL_1 | 167 | 175 | PF00134 | 0.518 |
DOC_CYCLIN_RxL_1 | 487 | 495 | PF00134 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.535 |
DOC_CYCLIN_yCln2_LP_2 | 324 | 330 | PF00134 | 0.417 |
DOC_MAPK_gen_1 | 10 | 17 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 234 | 243 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 82 | 90 | PF00069 | 0.490 |
DOC_MAPK_HePTP_8 | 322 | 334 | PF00069 | 0.419 |
DOC_MAPK_JIP1_4 | 235 | 241 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 171 | 178 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 234 | 243 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 325 | 334 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 612 | 620 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.432 |
DOC_MAPK_NFAT4_5 | 171 | 179 | PF00069 | 0.469 |
DOC_PP2B_LxvP_1 | 324 | 327 | PF13499 | 0.413 |
DOC_PP2B_LxvP_1 | 558 | 561 | PF13499 | 0.328 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.300 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.493 |
DOC_USP7_UBL2_3 | 234 | 238 | PF12436 | 0.361 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.255 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.482 |
LIG_14-3-3_CanoR_1 | 553 | 559 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 612 | 616 | PF00244 | 0.450 |
LIG_APCC_ABBA_1 | 423 | 428 | PF00400 | 0.376 |
LIG_BIR_III_4 | 36 | 40 | PF00653 | 0.496 |
LIG_BRCT_BRCA1_1 | 42 | 46 | PF00533 | 0.415 |
LIG_CaM_NSCaTE_8 | 177 | 184 | PF13499 | 0.455 |
LIG_Clathr_ClatBox_1 | 491 | 495 | PF01394 | 0.409 |
LIG_deltaCOP1_diTrp_1 | 285 | 292 | PF00928 | 0.462 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.450 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.414 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.426 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.557 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.304 |
LIG_LIR_Apic_2 | 409 | 414 | PF02991 | 0.300 |
LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 313 | 322 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 601 | 610 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 601 | 605 | PF02991 | 0.547 |
LIG_MYND_3 | 158 | 162 | PF01753 | 0.491 |
LIG_NRBOX | 357 | 363 | PF00104 | 0.360 |
LIG_Pex14_2 | 411 | 415 | PF04695 | 0.376 |
LIG_Pex14_2 | 422 | 426 | PF04695 | 0.376 |
LIG_PTB_Apo_2 | 494 | 501 | PF02174 | 0.300 |
LIG_SH2_CRK | 365 | 369 | PF00017 | 0.300 |
LIG_SH2_SRC | 565 | 568 | PF00017 | 0.300 |
LIG_SH2_SRC | 583 | 586 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.567 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.448 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.541 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.368 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 520 | 529 | PF11976 | 0.361 |
LIG_SUMO_SIM_anti_2 | 617 | 626 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 404 | 409 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 480 | 486 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 526 | 534 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 86 | 91 | PF11976 | 0.435 |
LIG_TRAF2_1 | 4 | 7 | PF00917 | 0.418 |
LIG_TRAF2_1 | 465 | 468 | PF00917 | 0.602 |
LIG_TRAF2_1 | 545 | 548 | PF00917 | 0.328 |
LIG_TRAF2_2 | 384 | 389 | PF00917 | 0.231 |
LIG_TYR_ITIM | 363 | 368 | PF00017 | 0.300 |
LIG_UBA3_1 | 173 | 180 | PF00899 | 0.463 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.541 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.653 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.572 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.542 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.452 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.369 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.727 |
MOD_CK1_1 | 614 | 620 | PF00069 | 0.316 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.449 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.518 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.580 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.587 |
MOD_Cter_Amidation | 232 | 235 | PF01082 | 0.403 |
MOD_Cter_Amidation | 585 | 588 | PF01082 | 0.626 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.443 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.482 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.612 |
MOD_GlcNHglycan | 308 | 312 | PF01048 | 0.664 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.368 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.464 |
MOD_GlcNHglycan | 467 | 472 | PF01048 | 0.630 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.583 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.453 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.297 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.569 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.574 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.581 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.501 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.591 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.471 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.602 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.586 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.282 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.722 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.478 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.474 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.300 |
MOD_N-GLC_1 | 593 | 598 | PF02516 | 0.523 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.419 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.550 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.336 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.336 |
MOD_NEK2_2 | 137 | 142 | PF00069 | 0.366 |
MOD_NEK2_2 | 578 | 583 | PF00069 | 0.748 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.588 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.388 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.376 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.667 |
MOD_PKA_2 | 611 | 617 | PF00069 | 0.409 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.413 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.488 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.325 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.543 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.300 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.565 |
MOD_Plk_2-3 | 285 | 291 | PF00069 | 0.411 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.434 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.352 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.300 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.654 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.533 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.401 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.392 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.455 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.416 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.673 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.481 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.255 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 357 | 362 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 487 | 492 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.300 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 587 | 590 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.463 |
TRG_NES_CRM1_1 | 216 | 230 | PF08389 | 0.352 |
TRG_NLS_Bipartite_1 | 82 | 103 | PF00514 | 0.367 |
TRG_NLS_MonoExtC_3 | 586 | 591 | PF00514 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 490 | 495 | PF00026 | 0.367 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P0J4 | Trypanosomatidae | 32% | 100% |
A0A3Q8IGM5 | Leishmania donovani | 92% | 100% |
A0A422NKA3 | Trypanosoma rangeli | 33% | 100% |
A4HQ69 | Leishmania braziliensis | 77% | 100% |
A4IDW7 | Leishmania infantum | 92% | 100% |
E9ATY8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |