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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HQ69
Term | Name | Level | Count |
---|---|---|---|
GO:0000993 | RNA polymerase II complex binding | 5 | 10 |
GO:0001098 | basal transcription machinery binding | 3 | 10 |
GO:0001099 | basal RNA polymerase II transcription machinery binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0008173 | RNA methyltransferase activity | 4 | 10 |
GO:0008174 | mRNA methyltransferase activity | 5 | 10 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 10 |
GO:0016422 | mRNA (2'-O-methyladenosine-N6-)-methyltransferase activity | 6 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 10 |
GO:0019899 | enzyme binding | 3 | 10 |
GO:0043175 | RNA polymerase core enzyme binding | 5 | 10 |
GO:0070063 | RNA polymerase binding | 4 | 10 |
GO:0099122 | RNA polymerase II C-terminal domain binding | 6 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.403 |
CLV_C14_Caspase3-7 | 264 | 268 | PF00656 | 0.507 |
CLV_C14_Caspase3-7 | 352 | 356 | PF00656 | 0.322 |
CLV_C14_Caspase3-7 | 477 | 481 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.443 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 591 | 593 | PF00082 | 0.659 |
CLV_PCSK_PC7_1 | 581 | 587 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.341 |
CLV_Separin_Metazoa | 582 | 586 | PF03568 | 0.506 |
CLV_Separin_Metazoa | 7 | 11 | PF03568 | 0.336 |
DEG_APCC_DBOX_1 | 103 | 111 | PF00400 | 0.427 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.461 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.475 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.434 |
DOC_CYCLIN_RxL_1 | 170 | 178 | PF00134 | 0.440 |
DOC_CYCLIN_yCln2_LP_2 | 160 | 166 | PF00134 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 326 | 332 | PF00134 | 0.376 |
DOC_MAPK_gen_1 | 10 | 17 | PF00069 | 0.383 |
DOC_MAPK_gen_1 | 23 | 31 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 325 | 334 | PF00069 | 0.244 |
DOC_MAPK_gen_1 | 82 | 90 | PF00069 | 0.502 |
DOC_MAPK_HePTP_8 | 322 | 334 | PF00069 | 0.375 |
DOC_MAPK_JIP1_4 | 238 | 244 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 174 | 181 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 238 | 246 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 325 | 334 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.376 |
DOC_MAPK_NFAT4_5 | 174 | 182 | PF00069 | 0.416 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.467 |
DOC_PP2B_LxvP_1 | 326 | 329 | PF13499 | 0.371 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.276 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.469 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.530 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.252 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 199 | 205 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 223 | 228 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 296 | 300 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 327 | 333 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.438 |
LIG_APCC_ABBA_1 | 31 | 36 | PF00400 | 0.358 |
LIG_APCC_ABBA_1 | 426 | 431 | PF00400 | 0.341 |
LIG_BIR_III_4 | 36 | 40 | PF00653 | 0.421 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.272 |
LIG_CaM_NSCaTE_8 | 180 | 187 | PF13499 | 0.411 |
LIG_Clathr_ClatBox_1 | 494 | 498 | PF01394 | 0.425 |
LIG_deltaCOP1_diTrp_1 | 287 | 294 | PF00928 | 0.485 |
LIG_deltaCOP1_diTrp_1 | 66 | 74 | PF00928 | 0.367 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.426 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.400 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.444 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.375 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.389 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.477 |
LIG_FHA_2 | 475 | 481 | PF00498 | 0.460 |
LIG_LIR_Apic_2 | 412 | 417 | PF02991 | 0.276 |
LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 285 | 295 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 313 | 324 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 612 | 619 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 612 | 616 | PF02991 | 0.363 |
LIG_MYND_3 | 161 | 165 | PF01753 | 0.463 |
LIG_NRBOX | 360 | 366 | PF00104 | 0.393 |
LIG_NRBOX | 4 | 10 | PF00104 | 0.310 |
LIG_PCNA_yPIPBox_3 | 114 | 122 | PF02747 | 0.275 |
LIG_PCNA_yPIPBox_3 | 2 | 12 | PF02747 | 0.253 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.444 |
LIG_Pex14_2 | 425 | 429 | PF04695 | 0.326 |
LIG_PTB_Apo_2 | 497 | 504 | PF02174 | 0.276 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.276 |
LIG_SH2_SRC | 568 | 571 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.276 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.477 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.649 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.460 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.288 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.190 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 331 | 336 | PF11976 | 0.292 |
LIG_SUMO_SIM_anti_2 | 529 | 538 | PF11976 | 0.298 |
LIG_SUMO_SIM_anti_2 | 620 | 628 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 407 | 412 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 529 | 538 | PF11976 | 0.397 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.420 |
LIG_TRAF2_1 | 4 | 7 | PF00917 | 0.382 |
LIG_TYR_ITIM | 366 | 371 | PF00017 | 0.276 |
LIG_UBA3_1 | 176 | 183 | PF00899 | 0.413 |
LIG_WW_3 | 561 | 565 | PF00397 | 0.199 |
MOD_CDC14_SPxK_1 | 403 | 406 | PF00782 | 0.286 |
MOD_CDK_SPK_2 | 135 | 140 | PF00069 | 0.379 |
MOD_CDK_SPxK_1 | 400 | 406 | PF00069 | 0.286 |
MOD_CDK_SPxxK_3 | 457 | 464 | PF00069 | 0.364 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.554 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.423 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.589 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.399 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.484 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.474 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.307 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.480 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.501 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.352 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.316 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.618 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.473 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.409 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.431 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.499 |
MOD_GlcNHglycan | 267 | 271 | PF01048 | 0.635 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.604 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.278 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.344 |
MOD_GlcNHglycan | 476 | 480 | PF01048 | 0.580 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.464 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.562 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.674 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.439 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.569 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.693 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.474 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.508 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.467 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.536 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.300 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.466 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.408 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.642 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.300 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.298 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.669 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.199 |
MOD_NEK2_2 | 53 | 58 | PF00069 | 0.390 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.547 |
MOD_PIKK_1 | 486 | 492 | PF00454 | 0.527 |
MOD_PIKK_1 | 535 | 541 | PF00454 | 0.225 |
MOD_PIKK_1 | 645 | 651 | PF00454 | 0.261 |
MOD_PK_1 | 140 | 146 | PF00069 | 0.463 |
MOD_PK_1 | 544 | 550 | PF00069 | 0.199 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.300 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.359 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.419 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.401 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.649 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.548 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.538 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.492 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.277 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.440 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.471 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.278 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.410 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.521 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.375 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.469 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.348 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.233 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.542 |
TRG_DiLeu_BaEn_4 | 19 | 25 | PF01217 | 0.292 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.300 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.341 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 584 | 586 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 218 | 222 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 546 | 550 | PF00026 | 0.275 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P0J4 | Trypanosomatidae | 31% | 100% |
A0A3Q8IGM5 | Leishmania donovani | 78% | 100% |
A0A422NKA3 | Trypanosoma rangeli | 33% | 100% |
A4IDW7 | Leishmania infantum | 78% | 100% |
E9ATY8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q0K8 | Leishmania major | 77% | 99% |
V5BF31 | Trypanosoma cruzi | 27% | 95% |
V5BTB5 | Trypanosoma cruzi | 32% | 100% |