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: A0A3S5H7N5
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 | 0.720 |
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.650 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.704 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.787 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.668 |
DEG_SCF_TRCP1_1 | 262 | 268 | PF00400 | 0.553 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.614 |
DEG_SPOP_SBC_1 | 254 | 258 | PF00917 | 0.775 |
DOC_CYCLIN_yCln2_LP_2 | 127 | 133 | PF00134 | 0.319 |
DOC_MAPK_gen_1 | 288 | 299 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 359 | 368 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 361 | 370 | PF00069 | 0.304 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.516 |
DOC_PP4_FxxP_1 | 215 | 218 | PF00568 | 0.343 |
DOC_PP4_FxxP_1 | 232 | 235 | PF00568 | 0.451 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 240 | 244 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 313 | 318 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 323 | 327 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 420 | 426 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 454 | 463 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 89 | 96 | PF00244 | 0.692 |
LIG_APCC_ABBA_1 | 478 | 483 | PF00400 | 0.538 |
LIG_BIR_III_2 | 461 | 465 | PF00653 | 0.557 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.606 |
LIG_Clathr_ClatBox_1 | 365 | 369 | PF01394 | 0.465 |
LIG_CtBP_PxDLS_1 | 154 | 158 | PF00389 | 0.620 |
LIG_CtBP_PxDLS_1 | 218 | 222 | PF00389 | 0.477 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.583 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.556 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.486 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.551 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.662 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.509 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.482 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.356 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.711 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.615 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.719 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.588 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 293 | 300 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 329 | 335 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.437 |
LIG_PCNA_TLS_4 | 403 | 412 | PF02747 | 0.504 |
LIG_PCNA_yPIPBox_3 | 282 | 291 | PF02747 | 0.475 |
LIG_PCNA_yPIPBox_3 | 67 | 81 | PF02747 | 0.704 |
LIG_Pex14_1 | 426 | 430 | PF04695 | 0.395 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.504 |
LIG_Pex14_2 | 438 | 442 | PF04695 | 0.523 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.305 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.368 |
LIG_SH2_PTP2 | 191 | 194 | PF00017 | 0.498 |
LIG_SH2_PTP2 | 296 | 299 | PF00017 | 0.388 |
LIG_SH2_PTP2 | 362 | 365 | PF00017 | 0.319 |
LIG_SH2_SRC | 191 | 194 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 423 | 427 | PF00017 | 0.405 |
LIG_SH2_STAT3 | 317 | 320 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.382 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.536 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.578 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.652 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.523 |
LIG_SUMO_SIM_par_1 | 296 | 304 | PF11976 | 0.441 |
LIG_TRAF2_1 | 63 | 66 | PF00917 | 0.560 |
LIG_TYR_ITIM | 209 | 214 | PF00017 | 0.356 |
LIG_UBA3_1 | 365 | 373 | PF00899 | 0.472 |
LIG_WRC_WIRS_1 | 406 | 411 | PF05994 | 0.455 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.586 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.663 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.622 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.495 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.641 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.590 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.679 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.742 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.490 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.609 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.505 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.564 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.650 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.766 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.592 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.486 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.567 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.666 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.424 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.675 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.716 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.553 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.712 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.588 |
MOD_NEK2_2 | 274 | 279 | PF00069 | 0.578 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.559 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.655 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.458 |
MOD_PKA_1 | 322 | 328 | PF00069 | 0.577 |
MOD_PKA_1 | 454 | 460 | PF00069 | 0.450 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.569 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.606 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.546 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.486 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.586 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.546 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.446 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.362 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.590 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.395 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.531 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.575 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.419 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.602 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.407 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.494 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.320 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.575 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.681 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.456 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.705 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.621 |
MOD_SUMO_rev_2 | 41 | 49 | PF00179 | 0.682 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.776 |
TRG_DiLeu_BaLyEn_6 | 361 | 366 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.381 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 453 | 455 | PF00400 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 364 | 369 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBI6 | Leptomonas seymouri | 47% | 99% |
A0A1X0P1I4 | Trypanosomatidae | 31% | 100% |
A0A1X0P1L0 | Trypanosomatidae | 31% | 100% |
A0A3R7NR23 | Trypanosoma rangeli | 31% | 100% |
A4HIJ0 | Leishmania braziliensis | 73% | 100% |
A4I5T4 | Leishmania infantum | 99% | 100% |
C9ZR56 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B129 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q736 | Leishmania major | 91% | 100% |
V5DNZ0 | Trypanosoma cruzi | 31% | 100% |