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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9B129
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009057 | macromolecule catabolic process | 4 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0030163 | protein catabolic process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008914 | leucyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016755 | aminoacyltransferase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.687 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.685 |
DEG_SPOP_SBC_1 | 255 | 259 | PF00917 | 0.743 |
DOC_CKS1_1 | 3 | 8 | PF01111 | 0.675 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.523 |
DOC_PP4_FxxP_1 | 216 | 219 | PF00568 | 0.343 |
DOC_PP4_FxxP_1 | 233 | 236 | PF00568 | 0.451 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.638 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.376 |
LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 241 | 245 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 314 | 319 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 324 | 328 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 421 | 427 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 455 | 464 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 90 | 97 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 98 | 105 | PF00244 | 0.657 |
LIG_APCC_ABBA_1 | 479 | 484 | PF00400 | 0.542 |
LIG_BIR_III_2 | 462 | 466 | PF00653 | 0.559 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.648 |
LIG_Clathr_ClatBox_1 | 366 | 370 | PF01394 | 0.474 |
LIG_CtBP_PxDLS_1 | 155 | 159 | PF00389 | 0.659 |
LIG_CtBP_PxDLS_1 | 219 | 223 | PF00389 | 0.477 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.610 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.561 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.483 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.545 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.662 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.478 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.477 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.362 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.720 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.718 |
LIG_LIR_Apic_2 | 149 | 155 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 330 | 336 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 394 | 398 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.462 |
LIG_PCNA_TLS_4 | 404 | 413 | PF02747 | 0.494 |
LIG_PCNA_yPIPBox_3 | 283 | 292 | PF02747 | 0.473 |
LIG_PCNA_yPIPBox_3 | 68 | 82 | PF02747 | 0.701 |
LIG_Pex14_1 | 427 | 431 | PF04695 | 0.392 |
LIG_Pex14_2 | 173 | 177 | PF04695 | 0.499 |
LIG_Pex14_2 | 439 | 443 | PF04695 | 0.516 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.306 |
LIG_SH2_CRK | 212 | 216 | PF00017 | 0.353 |
LIG_SH2_PTP2 | 192 | 195 | PF00017 | 0.505 |
LIG_SH2_SRC | 192 | 195 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.404 |
LIG_SH2_STAT3 | 318 | 321 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.388 |
LIG_SH3_2 | 3 | 8 | PF14604 | 0.597 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.536 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.585 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.633 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.522 |
LIG_SUMO_SIM_par_1 | 297 | 305 | PF11976 | 0.440 |
LIG_TRAF2_1 | 354 | 357 | PF00917 | 0.582 |
LIG_TYR_ITIM | 210 | 215 | PF00017 | 0.348 |
LIG_UBA3_1 | 366 | 374 | PF00899 | 0.477 |
LIG_WRC_WIRS_1 | 407 | 412 | PF05994 | 0.444 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.600 |
MOD_CDK_SPxxK_3 | 484 | 491 | PF00069 | 0.386 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.612 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.497 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.504 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.686 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.662 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.493 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.415 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.644 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.609 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.732 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.486 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.522 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.504 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.691 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.514 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.790 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.474 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.611 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.485 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.544 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.389 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.601 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.609 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.711 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.489 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.583 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.593 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.710 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.598 |
MOD_NEK2_2 | 275 | 280 | PF00069 | 0.577 |
MOD_PKA_1 | 323 | 329 | PF00069 | 0.572 |
MOD_PKA_1 | 455 | 461 | PF00069 | 0.450 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.613 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.511 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.581 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.378 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.448 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.553 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.354 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.438 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.531 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.659 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.373 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.414 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.399 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.266 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.383 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.640 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.712 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.466 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.678 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.681 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.538 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.380 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.623 |
MOD_SUMO_rev_2 | 40 | 50 | PF00179 | 0.711 |
TRG_DiLeu_BaEn_1 | 67 | 72 | PF01217 | 0.756 |
TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 365 | 370 | PF00026 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBI6 | Leptomonas seymouri | 47% | 99% |
A0A1X0P1I4 | Trypanosomatidae | 34% | 100% |
A0A1X0P1L0 | Trypanosomatidae | 34% | 100% |
A0A3R7NR23 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H7N5 | Leishmania donovani | 88% | 100% |
A4HIJ0 | Leishmania braziliensis | 73% | 99% |
A4I5T4 | Leishmania infantum | 88% | 100% |
C9ZR56 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
Q4Q736 | Leishmania major | 89% | 100% |
V5DNZ0 | Trypanosoma cruzi | 33% | 100% |