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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H4L6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008173 | RNA methyltransferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0008649 | rRNA methyltransferase activity | 5 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016435 | rRNA (guanine) methyltransferase activity | 6 | 1 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.404 |
CLV_PCSK_FUR_1 | 162 | 166 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.295 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.444 |
DEG_APCC_DBOX_1 | 197 | 205 | PF00400 | 0.425 |
DEG_SPOP_SBC_1 | 238 | 242 | PF00917 | 0.666 |
DEG_SPOP_SBC_1 | 244 | 248 | PF00917 | 0.610 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.565 |
DOC_CKS1_1 | 561 | 566 | PF01111 | 0.495 |
DOC_CYCLIN_RxL_1 | 416 | 427 | PF00134 | 0.500 |
DOC_CYCLIN_yCln2_LP_2 | 189 | 195 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 558 | 564 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 187 | 195 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 208 | 215 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 515 | 523 | PF00069 | 0.660 |
DOC_MAPK_MEF2A_6 | 187 | 195 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 517 | 525 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 80 | 87 | PF00069 | 0.543 |
DOC_PP1_SILK_1 | 283 | 288 | PF00149 | 0.562 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.537 |
DOC_PP2B_LxvP_1 | 189 | 192 | PF13499 | 0.524 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.733 |
LIG_14-3-3_CanoR_1 | 175 | 182 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 301 | 310 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 325 | 334 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 335 | 343 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 344 | 354 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 372 | 382 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 453 | 463 | PF00244 | 0.710 |
LIG_Actin_WH2_2 | 37 | 54 | PF00022 | 0.533 |
LIG_Actin_WH2_2 | 437 | 455 | PF00022 | 0.686 |
LIG_APCC_ABBA_1 | 63 | 68 | PF00400 | 0.505 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 329 | 333 | PF00533 | 0.513 |
LIG_CSL_BTD_1 | 561 | 564 | PF09270 | 0.490 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.701 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.639 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.527 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.765 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.490 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.491 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.444 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.344 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.543 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.470 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.659 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.648 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 560 | 565 | PF02991 | 0.585 |
LIG_MYND_1 | 101 | 105 | PF01753 | 0.547 |
LIG_MYND_1 | 566 | 570 | PF01753 | 0.520 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.534 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 220 | 223 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.490 |
LIG_SH3_2 | 102 | 107 | PF14604 | 0.395 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.721 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.319 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.515 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.502 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.525 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.496 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.408 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.525 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.480 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.544 |
LIG_SUMO_SIM_anti_2 | 355 | 362 | PF11976 | 0.585 |
LIG_SUMO_SIM_par_1 | 145 | 154 | PF11976 | 0.677 |
LIG_SxIP_EBH_1 | 23 | 32 | PF03271 | 0.585 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.593 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.408 |
LIG_WW_1 | 173 | 176 | PF00397 | 0.398 |
LIG_WW_1 | 35 | 38 | PF00397 | 0.596 |
LIG_WW_3 | 172 | 176 | PF00397 | 0.331 |
MOD_CDK_SPK_2 | 443 | 448 | PF00069 | 0.676 |
MOD_CDK_SPxxK_3 | 25 | 32 | PF00069 | 0.635 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.659 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.608 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.513 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.461 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.577 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.424 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.557 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.573 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.708 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.709 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.612 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.643 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.525 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.663 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.597 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.614 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.768 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.351 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.286 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.319 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.196 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.373 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.690 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.738 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.706 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.435 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.783 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.778 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.306 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.785 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.493 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.568 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.430 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.513 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.455 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.634 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.698 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.528 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.770 |
MOD_LATS_1 | 454 | 460 | PF00433 | 0.522 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.575 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.667 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.557 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.452 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.491 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.685 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.708 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.734 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.511 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.531 |
MOD_PIKK_1 | 479 | 485 | PF00454 | 0.524 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.412 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.596 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.529 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.642 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.487 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.496 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.577 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.594 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.669 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.599 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.461 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.585 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.528 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.524 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.404 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.589 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.650 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.423 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.483 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.733 |
TRG_DiLeu_BaLyEn_6 | 12 | 17 | PF01217 | 0.695 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.598 |
TRG_NLS_MonoExtN_4 | 165 | 172 | PF00514 | 0.675 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C1 | Leptomonas seymouri | 48% | 100% |
A0A1X0NKH6 | Trypanosomatidae | 30% | 100% |
A0A3R7KE58 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H5Q8 | Leishmania donovani | 73% | 100% |
A4HSU2 | Leishmania infantum | 73% | 100% |
C9ZTF4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AKS9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QJ28 | Leishmania major | 72% | 97% |
V5BT12 | Trypanosoma cruzi | 29% | 100% |