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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3Q8IFC1
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008171 | O-methyltransferase activity | 5 | 12 |
GO:0008173 | RNA methyltransferase activity | 4 | 12 |
GO:0008175 | tRNA methyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0062105 | RNA 2'-O-methyltransferase activity | 5 | 12 |
GO:0106050 | tRNA 2'-O-methyltransferase activity | 6 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.182 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.164 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.173 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.155 |
CLV_PCSK_PC1ET2_1 | 585 | 587 | PF00082 | 0.167 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.193 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.161 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.172 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.228 |
DEG_APCC_DBOX_1 | 406 | 414 | PF00400 | 0.419 |
DEG_APCC_DBOX_1 | 446 | 454 | PF00400 | 0.372 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 523 | 531 | PF00400 | 0.380 |
DEG_SCF_FBW7_1 | 389 | 395 | PF00400 | 0.341 |
DEG_SCF_FBW7_2 | 128 | 135 | PF00400 | 0.469 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.427 |
DOC_CKS1_1 | 386 | 391 | PF01111 | 0.361 |
DOC_CKS1_1 | 58 | 63 | PF01111 | 0.423 |
DOC_MAPK_DCC_7 | 49 | 58 | PF00069 | 0.411 |
DOC_MAPK_DCC_7 | 535 | 545 | PF00069 | 0.341 |
DOC_MAPK_gen_1 | 40 | 48 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 49 | 55 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 57 | 65 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 582 | 593 | PF00069 | 0.378 |
DOC_MAPK_HePTP_8 | 46 | 58 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 40 | 48 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 407 | 415 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 49 | 58 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 586 | 595 | PF00069 | 0.458 |
DOC_PP1_RVXF_1 | 590 | 596 | PF00149 | 0.458 |
DOC_PP2B_LxvP_1 | 543 | 546 | PF13499 | 0.392 |
DOC_PP4_FxxP_1 | 58 | 61 | PF00568 | 0.433 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.441 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.423 |
LIG_14-3-3_CanoR_1 | 103 | 111 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 216 | 222 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 319 | 327 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 419 | 426 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 447 | 457 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 166 | 182 | PF00022 | 0.416 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.384 |
LIG_BRCT_BRCA1_1 | 9 | 13 | PF00533 | 0.386 |
LIG_Clathr_ClatBox_1 | 410 | 414 | PF01394 | 0.394 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.396 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.369 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.471 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.437 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.461 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.503 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.416 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.451 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.330 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.444 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.416 |
LIG_HP1_1 | 409 | 413 | PF01393 | 0.458 |
LIG_Integrin_RGD_1 | 149 | 151 | PF01839 | 0.386 |
LIG_LIR_Gen_1 | 330 | 337 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 477 | 486 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 554 | 563 | PF02991 | 0.364 |
LIG_LIR_LC3C_4 | 245 | 248 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.264 |
LIG_Pex14_1 | 396 | 400 | PF04695 | 0.361 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.210 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.373 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.182 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.510 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.415 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.437 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.324 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.635 |
LIG_SH3_CIN85_PxpxPR_1 | 469 | 474 | PF14604 | 0.346 |
LIG_SUMO_SIM_anti_2 | 245 | 250 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 408 | 414 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 513 | 519 | PF11976 | 0.447 |
LIG_SxIP_EBH_1 | 465 | 474 | PF03271 | 0.341 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.439 |
LIG_TRAF2_1 | 553 | 556 | PF00917 | 0.442 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.598 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.484 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.324 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.485 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.461 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.492 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.405 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.442 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.429 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.468 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.530 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.372 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.642 |
MOD_Cter_Amidation | 580 | 583 | PF01082 | 0.172 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.379 |
MOD_GlcNHglycan | 221 | 225 | PF01048 | 0.297 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.501 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.415 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.309 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.274 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.294 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.209 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.146 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.476 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.695 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.387 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.412 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.436 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.544 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.381 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.418 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.461 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.482 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.474 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.451 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.445 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.409 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.264 |
MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.164 |
MOD_N-GLC_2 | 617 | 619 | PF02516 | 0.253 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.355 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.432 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.419 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.424 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.472 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.384 |
MOD_NEK2_2 | 271 | 276 | PF00069 | 0.458 |
MOD_OFUCOSY | 11 | 18 | PF10250 | 0.381 |
MOD_OFUCOSY | 490 | 497 | PF10250 | 0.180 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.491 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.441 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.440 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.358 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.372 |
MOD_PKA_1 | 419 | 425 | PF00069 | 0.361 |
MOD_PKA_1 | 77 | 83 | PF00069 | 0.475 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.331 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.612 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.331 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.395 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.369 |
MOD_PKB_1 | 57 | 65 | PF00069 | 0.429 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.364 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.364 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.364 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.384 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.394 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.312 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.530 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.595 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.396 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.372 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.467 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.371 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.425 |
TRG_DiLeu_BaEn_3 | 615 | 621 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_4 | 284 | 290 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 499 | 504 | PF01217 | 0.361 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.212 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 435 | 438 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.434 |
TRG_NLS_MonoExtC_3 | 581 | 586 | PF00514 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.373 |
TRG_Pf-PMV_PEXEL_1 | 586 | 590 | PF00026 | 0.251 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMP0 | Leptomonas seymouri | 57% | 100% |
A0A0S4IU97 | Bodo saltans | 34% | 100% |
A0A1X0NKZ4 | Trypanosomatidae | 37% | 100% |
A0A3R7N0X9 | Trypanosoma rangeli | 41% | 100% |
A4HJ30 | Leishmania braziliensis | 77% | 100% |
A4I6K9 | Leishmania infantum | 99% | 100% |
A7TSF4 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 21% | 100% |
C9ZN61 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9B1K2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q6L1 | Leishmania major | 91% | 100% |
V5BII3 | Trypanosoma cruzi | 40% | 100% |