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 |
Related structures:
AlphaFold database: E9ATY8
Term | Name | Level | Count |
---|---|---|---|
GO:0000993 | RNA polymerase II complex binding | 5 | 7 |
GO:0001098 | basal transcription machinery binding | 3 | 7 |
GO:0001099 | basal RNA polymerase II transcription machinery binding | 4 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005515 | protein binding | 2 | 7 |
GO:0008168 | methyltransferase activity | 4 | 7 |
GO:0008173 | RNA methyltransferase activity | 4 | 7 |
GO:0008174 | mRNA methyltransferase activity | 5 | 7 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 7 |
GO:0016422 | mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity | 6 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 7 |
GO:0019899 | enzyme binding | 3 | 7 |
GO:0043175 | RNA polymerase core enzyme binding | 5 | 7 |
GO:0070063 | RNA polymerase binding | 4 | 7 |
GO:0099122 | RNA polymerase II C-terminal domain binding | 6 | 7 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.363 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 587 | 589 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.479 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 589 | 591 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.369 |
CLV_Separin_Metazoa | 7 | 11 | PF03568 | 0.337 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.450 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.332 |
DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.458 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.410 |
DEG_SPOP_SBC_1 | 520 | 524 | PF00917 | 0.325 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.456 |
DOC_CKS1_1 | 146 | 151 | PF01111 | 0.463 |
DOC_CKS1_1 | 295 | 300 | PF01111 | 0.486 |
DOC_CYCLIN_RxL_1 | 167 | 175 | PF00134 | 0.471 |
DOC_CYCLIN_RxL_1 | 488 | 496 | PF00134 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 324 | 330 | PF00134 | 0.414 |
DOC_MAPK_gen_1 | 10 | 17 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 235 | 243 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 82 | 90 | PF00069 | 0.462 |
DOC_MAPK_HePTP_8 | 322 | 334 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 171 | 178 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 235 | 243 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 325 | 334 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.380 |
DOC_MAPK_NFAT4_5 | 171 | 179 | PF00069 | 0.451 |
DOC_PP2B_LxvP_1 | 324 | 327 | PF13499 | 0.406 |
DOC_PP2B_LxvP_1 | 559 | 562 | PF13499 | 0.325 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.304 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.484 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.261 |
LIG_14-3-3_CanoR_1 | 137 | 142 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.205 |
LIG_14-3-3_CanoR_1 | 554 | 560 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 613 | 617 | PF00244 | 0.427 |
LIG_APCC_ABBA_1 | 424 | 429 | PF00400 | 0.369 |
LIG_BIR_III_4 | 36 | 40 | PF00653 | 0.473 |
LIG_BRCT_BRCA1_1 | 42 | 46 | PF00533 | 0.387 |
LIG_Clathr_ClatBox_1 | 492 | 496 | PF01394 | 0.410 |
LIG_deltaCOP1_diTrp_1 | 285 | 292 | PF00928 | 0.448 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.449 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.447 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.369 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.253 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.284 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.270 |
LIG_LIR_Apic_2 | 410 | 415 | PF02991 | 0.304 |
LIG_LIR_Apic_2 | 73 | 77 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 313 | 322 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 602 | 611 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 602 | 606 | PF02991 | 0.559 |
LIG_MYND_3 | 158 | 162 | PF01753 | 0.456 |
LIG_NRBOX | 358 | 364 | PF00104 | 0.369 |
LIG_Pex14_2 | 412 | 416 | PF04695 | 0.369 |
LIG_Pex14_2 | 423 | 427 | PF04695 | 0.288 |
LIG_PTB_Apo_2 | 495 | 502 | PF02174 | 0.304 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.304 |
LIG_SH2_SRC | 566 | 569 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.335 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.432 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.370 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.316 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.482 |
LIG_SUMO_SIM_anti_2 | 521 | 530 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 618 | 627 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 405 | 410 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 527 | 535 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 86 | 91 | PF11976 | 0.429 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.314 |
LIG_TRAF2_1 | 4 | 7 | PF00917 | 0.412 |
LIG_TRAF2_1 | 466 | 469 | PF00917 | 0.598 |
LIG_TRAF2_1 | 546 | 549 | PF00917 | 0.325 |
LIG_TYR_ITIM | 364 | 369 | PF00017 | 0.352 |
LIG_UBA3_1 | 173 | 180 | PF00899 | 0.447 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.355 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.590 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.618 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.205 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.297 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.693 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.638 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.362 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.695 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.339 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.454 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.572 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.453 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.312 |
MOD_Cter_Amidation | 586 | 589 | PF01082 | 0.656 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.458 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.483 |
MOD_GlcNHglycan | 308 | 312 | PF01048 | 0.431 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.371 |
MOD_GlcNHglycan | 347 | 351 | PF01048 | 0.445 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.347 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.382 |
MOD_GlcNHglycan | 468 | 473 | PF01048 | 0.632 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.596 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.412 |
MOD_GlcNHglycan | 574 | 578 | PF01048 | 0.548 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.567 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.513 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.600 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.495 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.507 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.500 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.548 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.254 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.434 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.452 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.280 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.206 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.494 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.487 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.304 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.425 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.553 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.304 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.304 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.471 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.454 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.205 |
MOD_PIKK_1 | 484 | 490 | PF00454 | 0.581 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.369 |
MOD_PK_1 | 137 | 143 | PF00069 | 0.421 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.259 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.369 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.253 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.700 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.415 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.410 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.486 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.312 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.596 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.495 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.304 |
MOD_Plk_2-3 | 285 | 291 | PF00069 | 0.559 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.425 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.212 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.304 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.547 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.408 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.399 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.467 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.261 |
MOD_SUMO_rev_2 | 32 | 40 | PF00179 | 0.343 |
TRG_DiLeu_BaEn_4 | 19 | 25 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 358 | 363 | PF01217 | 0.369 |
TRG_DiLeu_BaLyEn_6 | 488 | 493 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 588 | 591 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.382 |
TRG_NLS_MonoExtC_3 | 587 | 592 | PF00514 | 0.665 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 491 | 496 | PF00026 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGM5 | Leishmania donovani | 88% | 100% |
A0A422NKA3 | Trypanosoma rangeli | 33% | 100% |
A4HQ69 | Leishmania braziliensis | 74% | 100% |
A4IDW7 | Leishmania infantum | 88% | 100% |
Q4Q0K8 | Leishmania major | 88% | 100% |