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. | yes | 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: A0A3S5H5Q8
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 | 168 | 170 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.691 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.434 |
DEG_APCC_DBOX_1 | 107 | 115 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.409 |
DEG_SPOP_SBC_1 | 309 | 313 | PF00917 | 0.565 |
DOC_CYCLIN_RxL_1 | 400 | 411 | PF00134 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 190 | 196 | PF00134 | 0.519 |
DOC_MAPK_gen_1 | 209 | 216 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 499 | 507 | PF00069 | 0.656 |
DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 359 | 368 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 501 | 509 | PF00069 | 0.519 |
DOC_PP1_SILK_1 | 266 | 271 | PF00149 | 0.562 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.510 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.582 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.697 |
LIG_14-3-3_CanoR_1 | 176 | 183 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 284 | 293 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 295 | 301 | PF00244 | 0.396 |
LIG_Actin_WH2_2 | 37 | 54 | PF00022 | 0.538 |
LIG_Actin_WH2_2 | 421 | 439 | PF00022 | 0.636 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.509 |
LIG_BRCT_BRCA1_1 | 312 | 316 | PF00533 | 0.513 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.651 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.496 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.488 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.672 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.473 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.531 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.496 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.564 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.526 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 221 | 224 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.469 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.516 |
LIG_SUMO_SIM_anti_2 | 339 | 346 | PF11976 | 0.597 |
LIG_SxIP_EBH_1 | 23 | 32 | PF03271 | 0.554 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.596 |
LIG_TRAF2_1 | 447 | 450 | PF00917 | 0.709 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.568 |
LIG_TYR_ITIM | 140 | 145 | PF00017 | 0.559 |
LIG_WW_1 | 35 | 38 | PF00397 | 0.599 |
MOD_CDK_SPK_2 | 427 | 432 | PF00069 | 0.615 |
MOD_CDK_SPxxK_3 | 25 | 32 | PF00069 | 0.607 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.588 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.539 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.534 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.389 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.763 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.768 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.696 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.799 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.525 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.666 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.779 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.481 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.630 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.363 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.468 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.572 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.718 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.763 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.778 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.725 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.720 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.771 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.788 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.712 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.493 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.658 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.400 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.477 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.728 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.640 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.636 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.543 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.708 |
MOD_N-GLC_2 | 396 | 398 | PF02516 | 0.585 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.631 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.668 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.551 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.446 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.475 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.602 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.395 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.712 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.719 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.559 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.521 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.490 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.577 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.685 |
MOD_PKB_1 | 357 | 365 | PF00069 | 0.563 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.614 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.455 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.789 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.746 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.516 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.546 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.522 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.406 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.700 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.582 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.578 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.697 |
TRG_DiLeu_BaLyEn_6 | 12 | 17 | PF01217 | 0.641 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.500 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.647 |
TRG_NLS_MonoExtN_4 | 168 | 173 | PF00514 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3C1 | Leptomonas seymouri | 49% | 100% |
A0A1X0NKH6 | Trypanosomatidae | 29% | 100% |
A0A3R7KE58 | Trypanosoma rangeli | 33% | 100% |
A4H4L6 | Leishmania braziliensis | 73% | 100% |
A4HSU2 | Leishmania infantum | 100% | 100% |
C9ZTF4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AKS9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QJ28 | Leishmania major | 93% | 100% |
V5BT12 | Trypanosoma cruzi | 31% | 100% |