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: E9AX46
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 | 0.464 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.704 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.294 |
CLV_PCSK_FUR_1 | 204 | 208 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.345 |
DEG_APCC_DBOX_1 | 33 | 41 | PF00400 | 0.410 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.581 |
DEG_SPOP_SBC_1 | 431 | 435 | PF00917 | 0.407 |
DOC_CKS1_1 | 214 | 219 | PF01111 | 0.580 |
DOC_CYCLIN_RxL_1 | 455 | 466 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 241 | 250 | PF00069 | 0.288 |
DOC_MAPK_JIP1_4 | 402 | 408 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 241 | 250 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 402 | 410 | PF00069 | 0.342 |
DOC_PP1_RVXF_1 | 282 | 289 | PF00149 | 0.270 |
DOC_PP1_RVXF_1 | 45 | 52 | PF00149 | 0.550 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.380 |
DOC_PP2B_LxvP_1 | 446 | 449 | PF13499 | 0.354 |
DOC_PP4_FxxP_1 | 347 | 350 | PF00568 | 0.173 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.472 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 291 | 296 | PF00244 | 0.328 |
LIG_Clathr_ClatBox_1 | 405 | 409 | PF01394 | 0.332 |
LIG_deltaCOP1_diTrp_1 | 527 | 536 | PF00928 | 0.426 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.399 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.259 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.279 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.348 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.664 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.396 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.436 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.421 |
LIG_LIR_Apic_2 | 346 | 350 | PF02991 | 0.173 |
LIG_LIR_Apic_2 | 498 | 503 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 577 | 583 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 249 | 260 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 418 | 428 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 443 | 450 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 526 | 537 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 443 | 447 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 577 | 582 | PF02991 | 0.585 |
LIG_NRBOX | 415 | 421 | PF00104 | 0.469 |
LIG_PCNA_yPIPBox_3 | 55 | 69 | PF02747 | 0.364 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.279 |
LIG_Pex14_2 | 532 | 536 | PF04695 | 0.409 |
LIG_SH2_NCK_1 | 160 | 164 | PF00017 | 0.367 |
LIG_SH2_PTP2 | 444 | 447 | PF00017 | 0.314 |
LIG_SH2_PTP2 | 580 | 583 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.244 |
LIG_SH2_STAT3 | 144 | 147 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.490 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.412 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.376 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.532 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.466 |
LIG_SUMO_SIM_anti_2 | 22 | 27 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 443 | 449 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 402 | 407 | PF11976 | 0.338 |
LIG_TYR_ITIM | 442 | 447 | PF00017 | 0.390 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.459 |
MOD_CDK_SPxxK_3 | 566 | 573 | PF00069 | 0.493 |
MOD_CDK_SPxxK_3 | 583 | 590 | PF00069 | 0.424 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.476 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.500 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.283 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.492 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.688 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.626 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.560 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.530 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.429 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.440 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.520 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.768 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.512 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.498 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.371 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.279 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.297 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.567 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.629 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.713 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.687 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.173 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.430 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.590 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.674 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.564 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.515 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.377 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.694 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.551 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.484 |
MOD_NEK2_2 | 575 | 580 | PF00069 | 0.474 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.411 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.387 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.534 |
MOD_PK_1 | 150 | 156 | PF00069 | 0.401 |
MOD_PKA_1 | 2 | 8 | PF00069 | 0.709 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.709 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.374 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.568 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.418 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.579 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.337 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.354 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.434 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.453 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.307 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.279 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.697 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.493 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.601 |
MOD_SUMO_for_1 | 456 | 459 | PF00179 | 0.464 |
MOD_SUMO_rev_2 | 394 | 404 | PF00179 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 400 | 405 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 572 | 574 | PF00400 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 284 | 289 | PF00026 | 0.270 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1II31 | Leptomonas seymouri | 63% | 98% |
A0A1X0NXA7 | Trypanosomatidae | 45% | 100% |
A0A3Q8IBG9 | Leishmania donovani | 93% | 100% |
A0A422NWV1 | Trypanosoma rangeli | 47% | 100% |
A4HDR2 | Leishmania braziliensis | 82% | 100% |
A4I108 | Leishmania infantum | 93% | 100% |
C9ZWA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
Q4QAD0 | Leishmania major | 92% | 100% |
V5BAG8 | Trypanosoma cruzi | 46% | 100% |