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: E9AZB6
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 | 218 | 222 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.794 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.517 |
CLV_PCSK_FUR_1 | 344 | 348 | PF00082 | 0.629 |
CLV_PCSK_FUR_1 | 357 | 361 | PF00082 | 0.674 |
CLV_PCSK_FUR_1 | 370 | 374 | PF00082 | 0.737 |
CLV_PCSK_FUR_1 | 392 | 396 | PF00082 | 0.557 |
CLV_PCSK_FUR_1 | 405 | 409 | PF00082 | 0.760 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.291 |
CLV_PCSK_PC7_1 | 220 | 226 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 340 | 346 | PF00082 | 0.612 |
CLV_PCSK_PC7_1 | 357 | 363 | PF00082 | 0.712 |
CLV_PCSK_PC7_1 | 390 | 396 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 401 | 407 | PF00082 | 0.633 |
CLV_PCSK_PC7_1 | 417 | 423 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.244 |
DEG_APCC_DBOX_1 | 150 | 158 | PF00400 | 0.459 |
DOC_CYCLIN_RxL_1 | 185 | 195 | PF00134 | 0.514 |
DOC_MAPK_gen_1 | 134 | 142 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 237 | 244 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 306 | 315 | PF00069 | 0.676 |
DOC_MAPK_MEF2A_6 | 237 | 246 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 275 | 282 | PF00069 | 0.514 |
DOC_PP2B_PxIxI_1 | 275 | 281 | PF00149 | 0.491 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.514 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.514 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.474 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.588 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.532 |
LIG_BIR_III_4 | 102 | 106 | PF00653 | 0.673 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.276 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.449 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.496 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.534 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.654 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 51 | 57 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.460 |
LIG_MAD2 | 139 | 147 | PF02301 | 0.374 |
LIG_NRP_CendR_1 | 421 | 423 | PF00754 | 0.678 |
LIG_REV1ctd_RIR_1 | 21 | 30 | PF16727 | 0.447 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.480 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.459 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.518 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.514 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.459 |
LIG_TRFH_1 | 167 | 171 | PF08558 | 0.454 |
LIG_WW_3 | 207 | 211 | PF00397 | 0.598 |
LIG_WW_3 | 402 | 406 | PF00397 | 0.743 |
LIG_WW_3 | 412 | 416 | PF00397 | 0.686 |
LIG_WW_3 | 418 | 422 | PF00397 | 0.651 |
MOD_CDC14_SPxK_1 | 402 | 405 | PF00782 | 0.583 |
MOD_CDC14_SPxK_1 | 412 | 415 | PF00782 | 0.591 |
MOD_CDC14_SPxK_1 | 418 | 421 | PF00782 | 0.580 |
MOD_CDK_SPxK_1 | 399 | 405 | PF00069 | 0.586 |
MOD_CDK_SPxK_1 | 409 | 415 | PF00069 | 0.599 |
MOD_CDK_SPxxK_3 | 399 | 406 | PF00069 | 0.636 |
MOD_CDK_SPxxK_3 | 415 | 422 | PF00069 | 0.612 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.488 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.560 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.623 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.617 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.510 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.517 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.460 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.527 |
MOD_DYRK1A_RPxSP_1 | 399 | 403 | PF00069 | 0.587 |
MOD_DYRK1A_RPxSP_1 | 415 | 419 | PF00069 | 0.598 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.551 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.659 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.714 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.319 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.638 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.276 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.262 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.465 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.273 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.387 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.195 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.521 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.491 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.578 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.489 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.600 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.449 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.660 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.639 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.514 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.414 |
MOD_LATS_1 | 393 | 399 | PF00433 | 0.625 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.452 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.538 |
MOD_PKA_1 | 347 | 353 | PF00069 | 0.543 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.666 |
MOD_PKA_1 | 372 | 378 | PF00069 | 0.620 |
MOD_PKA_1 | 395 | 401 | PF00069 | 0.654 |
MOD_PKA_1 | 407 | 413 | PF00069 | 0.527 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.669 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.692 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.666 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.620 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.654 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.527 |
MOD_PKB_1 | 345 | 353 | PF00069 | 0.620 |
MOD_PKB_1 | 360 | 368 | PF00069 | 0.667 |
MOD_PKB_1 | 370 | 378 | PF00069 | 0.452 |
MOD_PKB_1 | 380 | 388 | PF00069 | 0.763 |
MOD_PKB_1 | 405 | 413 | PF00069 | 0.651 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.491 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.413 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.488 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.459 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.491 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.586 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.599 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.514 |
MOD_SUMO_for_1 | 307 | 310 | PF00179 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 311 | 316 | PF01217 | 0.521 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.794 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 404 | 407 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 420 | 423 | PF00400 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMB5 | Leptomonas seymouri | 50% | 100% |
A0A3R7LQ31 | Trypanosoma rangeli | 32% | 97% |
A0A3S7X0Y2 | Leishmania donovani | 94% | 93% |
A4HFY7 | Leishmania braziliensis | 80% | 100% |
A4I2Y0 | Leishmania infantum | 94% | 94% |
C9ZJH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 96% |
E9ADJ0 | Leishmania major | 94% | 100% |