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: 6 |
Silverman et al. | no | yes: 3 |
Pissara et al. | no | yes: 30 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IFP2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 23 |
GO:0016787 | hydrolase activity | 2 | 23 |
GO:0005488 | binding | 1 | 1 |
GO:0005506 | iron ion binding | 6 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.428 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 453 | 455 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.288 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.382 |
DEG_APCC_DBOX_1 | 340 | 348 | PF00400 | 0.292 |
DOC_ANK_TNKS_1 | 205 | 212 | PF00023 | 0.376 |
DOC_ANK_TNKS_1 | 307 | 314 | PF00023 | 0.286 |
DOC_MAPK_FxFP_2 | 49 | 52 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 279 | 287 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 7 | 16 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 70 | 78 | PF00069 | 0.407 |
DOC_MAPK_JIP1_4 | 19 | 25 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 175 | 183 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 281 | 289 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 428 | 437 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 7 | 16 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 70 | 78 | PF00069 | 0.407 |
DOC_PP1_RVXF_1 | 463 | 469 | PF00149 | 0.314 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.412 |
DOC_PP2B_LxvP_1 | 545 | 548 | PF13499 | 0.271 |
DOC_PP4_FxxP_1 | 405 | 408 | PF00568 | 0.364 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.444 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.406 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.313 |
DOC_USP7_UBL2_3 | 465 | 469 | PF12436 | 0.419 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.407 |
LIG_14-3-3_CanoR_1 | 108 | 112 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 428 | 434 | PF00244 | 0.310 |
LIG_APCC_ABBA_1 | 518 | 523 | PF00400 | 0.286 |
LIG_BRCT_BRCA1_1 | 132 | 136 | PF00533 | 0.466 |
LIG_EH1_1 | 525 | 533 | PF00400 | 0.298 |
LIG_EVH1_1 | 39 | 43 | PF00568 | 0.420 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.436 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.341 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.289 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.340 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.223 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.306 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.307 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.293 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.300 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.421 |
LIG_LIR_Apic_2 | 46 | 52 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 124 | 134 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 166 | 172 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 176 | 184 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 231 | 242 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 295 | 303 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 543 | 550 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 92 | 102 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 543 | 547 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.482 |
LIG_LRP6_Inhibitor_1 | 422 | 428 | PF00058 | 0.372 |
LIG_MYND_1 | 203 | 207 | PF01753 | 0.289 |
LIG_MYND_1 | 480 | 484 | PF01753 | 0.300 |
LIG_NRBOX | 21 | 27 | PF00104 | 0.424 |
LIG_Pex14_2 | 136 | 140 | PF04695 | 0.495 |
LIG_Pex14_2 | 380 | 384 | PF04695 | 0.314 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.375 |
LIG_SH2_PTP2 | 126 | 129 | PF00017 | 0.356 |
LIG_SH2_SRC | 126 | 129 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 298 | 302 | PF00017 | 0.300 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.249 |
LIG_SH2_STAT3 | 502 | 505 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.393 |
LIG_SH3_1 | 201 | 207 | PF00018 | 0.289 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.290 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.330 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.512 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.410 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.369 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.291 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.285 |
LIG_TRFH_1 | 16 | 20 | PF08558 | 0.381 |
LIG_TYR_ITIM | 165 | 170 | PF00017 | 0.405 |
LIG_UBA3_1 | 343 | 351 | PF00899 | 0.364 |
LIG_WRC_WIRS_1 | 91 | 96 | PF05994 | 0.349 |
LIG_WW_3 | 4 | 8 | PF00397 | 0.388 |
MOD_CDC14_SPxK_1 | 4 | 7 | PF00782 | 0.391 |
MOD_CDC14_SPxK_1 | 68 | 71 | PF00782 | 0.420 |
MOD_CDK_SPK_2 | 565 | 570 | PF00069 | 0.393 |
MOD_CDK_SPK_2 | 65 | 70 | PF00069 | 0.401 |
MOD_CDK_SPxK_1 | 1 | 7 | PF00069 | 0.422 |
MOD_CDK_SPxK_1 | 65 | 71 | PF00069 | 0.425 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.324 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.429 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.389 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.300 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.425 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.358 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.464 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.403 |
MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.300 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.298 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.295 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.444 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.360 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.428 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.280 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.323 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.442 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.310 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.424 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.544 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.383 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.378 |
MOD_N-GLC_2 | 475 | 477 | PF02516 | 0.370 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.327 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.271 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.379 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.353 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.333 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.299 |
MOD_NEK2_1 | 553 | 558 | PF00069 | 0.388 |
MOD_NEK2_2 | 464 | 469 | PF00069 | 0.463 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.378 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.435 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.433 |
MOD_PKA_1 | 70 | 76 | PF00069 | 0.384 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.362 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.413 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.408 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.363 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.407 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.439 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.286 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.356 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.371 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.422 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.388 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.348 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.364 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.443 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.407 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.407 |
MOD_SUMO_for_1 | 443 | 446 | PF00179 | 0.286 |
MOD_SUMO_rev_2 | 345 | 352 | PF00179 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 83 | 88 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.300 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.394 |
TRG_NES_CRM1_1 | 280 | 292 | PF08389 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 454 | 459 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Q9 | Leptomonas seymouri | 75% | 100% |
A0A0N1PBD8 | Leptomonas seymouri | 77% | 100% |
A0A0S4JJE7 | Bodo saltans | 60% | 100% |
A0A1X0P1Q0 | Trypanosomatidae | 63% | 100% |
A0A381MQ29 | Leishmania infantum | 100% | 100% |
A0A3R7KSZ4 | Trypanosoma rangeli | 63% | 100% |
A0A3S7X4P6 | Leishmania donovani | 100% | 100% |
A0A3S7X6U2 | Leishmania donovani | 75% | 100% |
A4HJG9 | Leishmania braziliensis | 92% | 100% |
A4HJH1 | Leishmania braziliensis | 92% | 100% |
A4HJI4 | Leishmania braziliensis | 92% | 100% |
A4HLM2 | Leishmania braziliensis | 71% | 100% |
A4I933 | Leishmania infantum | 75% | 100% |
B2KZE7 | Corynebacterium striatum | 28% | 100% |
C9ZQ48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
D0A536 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9B201 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B3Z8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q426 | Leishmania major | 74% | 100% |
Q4Q660 | Leishmania major | 95% | 100% |
Q4Q673 | Leishmania major | 95% | 100% |
Q6Q0N1 | Rattus norvegicus | 27% | 100% |
Q9D1A2 | Mus musculus | 26% | 100% |
Q9P6I2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
V5BHA2 | Trypanosoma cruzi | 62% | 100% |