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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016604 | nuclear body | 2 | 2 |
GO:0016607 | nuclear speck | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ADJ0
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 2 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008380 | RNA splicing | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.705 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.799 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.508 |
CLV_PCSK_FUR_1 | 344 | 348 | PF00082 | 0.753 |
CLV_PCSK_FUR_1 | 357 | 361 | PF00082 | 0.543 |
CLV_PCSK_FUR_1 | 370 | 374 | PF00082 | 0.653 |
CLV_PCSK_FUR_1 | 380 | 384 | PF00082 | 0.627 |
CLV_PCSK_FUR_1 | 392 | 396 | PF00082 | 0.574 |
CLV_PCSK_FUR_1 | 415 | 419 | PF00082 | 0.775 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.284 |
CLV_PCSK_PC7_1 | 220 | 226 | PF00082 | 0.613 |
CLV_PCSK_PC7_1 | 340 | 346 | PF00082 | 0.748 |
CLV_PCSK_PC7_1 | 357 | 363 | PF00082 | 0.483 |
CLV_PCSK_PC7_1 | 390 | 396 | PF00082 | 0.607 |
CLV_PCSK_PC7_1 | 401 | 407 | PF00082 | 0.640 |
CLV_PCSK_PC7_1 | 411 | 417 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 433 | 439 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.237 |
DEG_APCC_DBOX_1 | 150 | 158 | PF00400 | 0.452 |
DOC_ANK_TNKS_1 | 209 | 216 | PF00023 | 0.500 |
DOC_CYCLIN_RxL_1 | 185 | 193 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 134 | 142 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 237 | 244 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 306 | 315 | PF00069 | 0.649 |
DOC_MAPK_MEF2A_6 | 237 | 246 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 275 | 282 | PF00069 | 0.523 |
DOC_PP2B_PxIxI_1 | 275 | 281 | PF00149 | 0.484 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.523 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.523 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.523 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.485 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.582 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.544 |
LIG_BIR_III_4 | 102 | 106 | PF00653 | 0.683 |
LIG_BIR_III_4 | 212 | 216 | PF00653 | 0.511 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.269 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.442 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.507 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.538 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.653 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 51 | 57 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.453 |
LIG_MAD2 | 139 | 147 | PF02301 | 0.391 |
LIG_NRP_CendR_1 | 437 | 439 | PF00754 | 0.683 |
LIG_REV1ctd_RIR_1 | 21 | 30 | PF16727 | 0.440 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.468 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.452 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.590 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.523 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.452 |
LIG_TRFH_1 | 167 | 171 | PF08558 | 0.440 |
LIG_WW_3 | 207 | 211 | PF00397 | 0.580 |
LIG_WW_3 | 412 | 416 | PF00397 | 0.744 |
LIG_WW_3 | 422 | 426 | PF00397 | 0.549 |
LIG_WW_3 | 428 | 432 | PF00397 | 0.625 |
LIG_WW_3 | 434 | 438 | PF00397 | 0.568 |
MOD_CDC14_SPxK_1 | 402 | 405 | PF00782 | 0.615 |
MOD_CDC14_SPxK_1 | 412 | 415 | PF00782 | 0.580 |
MOD_CDC14_SPxK_1 | 422 | 425 | PF00782 | 0.592 |
MOD_CDC14_SPxK_1 | 428 | 431 | PF00782 | 0.591 |
MOD_CDC14_SPxK_1 | 434 | 437 | PF00782 | 0.554 |
MOD_CDK_SPxK_1 | 399 | 405 | PF00069 | 0.619 |
MOD_CDK_SPxK_1 | 409 | 415 | PF00069 | 0.582 |
MOD_CDK_SPxK_1 | 419 | 425 | PF00069 | 0.599 |
MOD_CDK_SPxK_1 | 431 | 437 | PF00069 | 0.585 |
MOD_CDK_SPxxK_3 | 399 | 406 | PF00069 | 0.754 |
MOD_CDK_SPxxK_3 | 409 | 416 | PF00069 | 0.654 |
MOD_CDK_SPxxK_3 | 431 | 438 | PF00069 | 0.658 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.502 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.538 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.564 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.610 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.550 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.520 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.526 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.458 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.513 |
MOD_DYRK1A_RPxSP_1 | 399 | 403 | PF00069 | 0.625 |
MOD_DYRK1A_RPxSP_1 | 409 | 413 | PF00069 | 0.585 |
MOD_DYRK1A_RPxSP_1 | 425 | 429 | PF00069 | 0.604 |
MOD_DYRK1A_RPxSP_1 | 431 | 435 | PF00069 | 0.611 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.562 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.681 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.732 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.328 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.647 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.273 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.233 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.266 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.386 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.198 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.537 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.534 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.503 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.679 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.621 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.650 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.641 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.664 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.665 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.523 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.396 |
MOD_LATS_1 | 393 | 399 | PF00433 | 0.588 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.581 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.494 |
MOD_PKA_1 | 338 | 344 | PF00069 | 0.579 |
MOD_PKA_1 | 347 | 353 | PF00069 | 0.724 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.498 |
MOD_PKA_1 | 372 | 378 | PF00069 | 0.574 |
MOD_PKA_1 | 382 | 388 | PF00069 | 0.505 |
MOD_PKA_1 | 395 | 401 | PF00069 | 0.553 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.658 |
MOD_PKA_1 | 417 | 423 | PF00069 | 0.539 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.616 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.533 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.669 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.645 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.498 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.574 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.505 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.553 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.658 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.539 |
MOD_PKB_1 | 345 | 353 | PF00069 | 0.736 |
MOD_PKB_1 | 360 | 368 | PF00069 | 0.504 |
MOD_PKB_1 | 370 | 378 | PF00069 | 0.571 |
MOD_PKB_1 | 380 | 388 | PF00069 | 0.593 |
MOD_PKB_1 | 415 | 423 | PF00069 | 0.647 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.484 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.502 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.452 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.484 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.629 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.582 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.599 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.585 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.523 |
MOD_SUMO_for_1 | 307 | 310 | PF00179 | 0.396 |
TRG_DiLeu_BaLyEn_6 | 311 | 316 | PF01217 | 0.507 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 424 | 427 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 430 | 433 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 436 | 439 | PF00400 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMB5 | Leptomonas seymouri | 51% | 100% |
A0A1X0NSK5 | Trypanosomatidae | 29% | 95% |
A0A3R7LQ31 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X0Y2 | Leishmania donovani | 98% | 97% |
A4HFY7 | Leishmania braziliensis | 81% | 100% |
A4I2Y0 | Leishmania infantum | 98% | 98% |
C9ZJH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AZB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |