Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016604 | nuclear body | 2 | 1 |
GO:0016607 | nuclear speck | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HFY7
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 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:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0008270 | zinc ion binding | 6 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0046914 | transition metal ion binding | 5 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.671 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.587 |
CLV_PCSK_FUR_1 | 348 | 352 | PF00082 | 0.597 |
CLV_PCSK_FUR_1 | 361 | 365 | PF00082 | 0.468 |
CLV_PCSK_FUR_1 | 376 | 380 | PF00082 | 0.587 |
CLV_PCSK_FUR_1 | 398 | 402 | PF00082 | 0.756 |
CLV_PCSK_FUR_1 | 408 | 412 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.519 |
CLV_PCSK_PC7_1 | 348 | 354 | PF00082 | 0.570 |
CLV_PCSK_PC7_1 | 361 | 367 | PF00082 | 0.441 |
CLV_PCSK_PC7_1 | 394 | 400 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.244 |
DOC_CYCLIN_RxL_1 | 189 | 199 | PF00134 | 0.514 |
DOC_MAPK_gen_1 | 138 | 146 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 240 | 248 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 310 | 319 | PF00069 | 0.640 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 279 | 286 | PF00069 | 0.514 |
DOC_PP2B_PxIxI_1 | 279 | 285 | PF00149 | 0.491 |
DOC_PP4_FxxP_1 | 265 | 268 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 58 | 61 | PF00568 | 0.514 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 191 | 195 | PF12436 | 0.394 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.591 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.540 |
LIG_BIR_III_4 | 106 | 110 | PF00653 | 0.592 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.440 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.276 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.394 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.639 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.449 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.556 |
LIG_LIR_Apic_2 | 274 | 280 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 55 | 61 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.460 |
LIG_MAD2 | 143 | 151 | PF02301 | 0.374 |
LIG_REV1ctd_RIR_1 | 21 | 30 | PF16727 | 0.447 |
LIG_SH2_PTP2 | 277 | 280 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.489 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.523 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.606 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.514 |
LIG_WW_3 | 211 | 215 | PF00397 | 0.575 |
LIG_WW_3 | 395 | 399 | PF00397 | 0.673 |
MOD_CDC14_SPxK_1 | 395 | 398 | PF00782 | 0.739 |
MOD_CDC14_SPxK_1 | 405 | 408 | PF00782 | 0.539 |
MOD_CDK_SPxK_1 | 392 | 398 | PF00069 | 0.706 |
MOD_CDK_SPxK_1 | 402 | 408 | PF00069 | 0.591 |
MOD_CDK_SPxxK_3 | 392 | 399 | PF00069 | 0.539 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.602 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.497 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.426 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.478 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.587 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.421 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.510 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.517 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.503 |
MOD_DYRK1A_RPxSP_1 | 392 | 396 | PF00069 | 0.699 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.555 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.319 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.761 |
MOD_GlcNHglycan | 215 | 220 | PF01048 | 0.754 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.630 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.296 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.240 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.387 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.230 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.550 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.568 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.568 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.497 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.749 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.394 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.565 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.595 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.778 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.687 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.624 |
MOD_LATS_1 | 349 | 355 | PF00433 | 0.461 |
MOD_LATS_1 | 402 | 408 | PF00433 | 0.522 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.526 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.194 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.483 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.452 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.483 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.513 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.451 |
MOD_PKA_1 | 351 | 357 | PF00069 | 0.541 |
MOD_PKA_1 | 366 | 372 | PF00069 | 0.572 |
MOD_PKA_1 | 377 | 383 | PF00069 | 0.584 |
MOD_PKA_1 | 388 | 394 | PF00069 | 0.774 |
MOD_PKA_1 | 400 | 406 | PF00069 | 0.687 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.627 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.517 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.604 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.646 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.572 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.584 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.774 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.687 |
MOD_PKB_1 | 350 | 358 | PF00069 | 0.585 |
MOD_PKB_1 | 364 | 372 | PF00069 | 0.442 |
MOD_PKB_1 | 377 | 385 | PF00069 | 0.590 |
MOD_PKB_1 | 398 | 406 | PF00069 | 0.654 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.579 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.497 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.394 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.394 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.491 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.706 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.591 |
MOD_SUMO_for_1 | 278 | 281 | PF00179 | 0.514 |
MOD_SUMO_for_1 | 311 | 314 | PF00179 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 315 | 320 | PF01217 | 0.509 |
TRG_ER_diArg_1 | 130 | 132 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 348 | 351 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 408 | 411 | PF00400 | 0.583 |
TRG_NLS_Bipartite_1 | 223 | 244 | PF00514 | 0.482 |
TRG_NLS_MonoExtC_3 | 239 | 245 | PF00514 | 0.421 |
TRG_NLS_MonoExtN_4 | 239 | 244 | PF00514 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMB5 | Leptomonas seymouri | 48% | 100% |
A0A1X0NSK5 | Trypanosomatidae | 28% | 91% |
A0A3R7LQ31 | Trypanosoma rangeli | 29% | 95% |
A0A3S7X0Y2 | Leishmania donovani | 81% | 92% |
A4I2Y0 | Leishmania infantum | 81% | 93% |
E9ADJ0 | Leishmania major | 81% | 100% |
E9AZB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |