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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HJK9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043171 | peptide catabolic process | 4 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004177 | aminopeptidase activity | 5 | 10 |
GO:0005488 | binding | 1 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008237 | metallopeptidase activity | 4 | 11 |
GO:0008238 | exopeptidase activity | 4 | 10 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0008235 | metalloexopeptidase activity | 5 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0042277 | peptide binding | 3 | 1 |
GO:0070006 | metalloaminopeptidase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.768 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 593 | 595 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.475 |
CLV_PCSK_FUR_1 | 41 | 45 | PF00082 | 0.448 |
CLV_PCSK_FUR_1 | 77 | 81 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 593 | 595 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.728 |
CLV_PCSK_PC7_1 | 362 | 368 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.482 |
CLV_Separin_Metazoa | 590 | 594 | PF03568 | 0.386 |
DEG_APCC_DBOX_1 | 607 | 615 | PF00400 | 0.296 |
DEG_SPOP_SBC_1 | 519 | 523 | PF00917 | 0.323 |
DEG_SPOP_SBC_1 | 55 | 59 | PF00917 | 0.505 |
DOC_CYCLIN_RxL_1 | 375 | 385 | PF00134 | 0.470 |
DOC_CYCLIN_yCln2_LP_2 | 474 | 480 | PF00134 | 0.259 |
DOC_MAPK_gen_1 | 593 | 601 | PF00069 | 0.391 |
DOC_PP1_RVXF_1 | 188 | 195 | PF00149 | 0.358 |
DOC_PP1_RVXF_1 | 261 | 267 | PF00149 | 0.386 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 474 | 477 | PF13499 | 0.259 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.290 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.290 |
DOC_PP4_FxxP_1 | 514 | 517 | PF00568 | 0.313 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.294 |
DOC_USP7_UBL2_3 | 499 | 503 | PF12436 | 0.308 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.208 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 370 | 379 | PF00244 | 0.447 |
LIG_APCC_ABBA_1 | 200 | 205 | PF00400 | 0.393 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 510 | 514 | PF00533 | 0.313 |
LIG_Clathr_ClatBox_1 | 191 | 195 | PF01394 | 0.470 |
LIG_CSL_BTD_1 | 7 | 10 | PF09270 | 0.240 |
LIG_deltaCOP1_diTrp_1 | 186 | 194 | PF00928 | 0.468 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.375 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.502 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.452 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.420 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.494 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.425 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.347 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.677 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.290 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.419 |
LIG_LIR_Apic_2 | 511 | 517 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 275 | 281 | PF02991 | 0.218 |
LIG_LIR_Gen_1 | 314 | 322 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 558 | 568 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 70 | 76 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 314 | 318 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.537 |
LIG_NRBOX | 405 | 411 | PF00104 | 0.383 |
LIG_NRBOX | 567 | 573 | PF00104 | 0.208 |
LIG_PAM2_1 | 178 | 190 | PF00658 | 0.378 |
LIG_PDZ_Class_1 | 613 | 618 | PF00595 | 0.505 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.393 |
LIG_SH2_GRB2like | 72 | 75 | PF00017 | 0.347 |
LIG_SH2_SRC | 545 | 548 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.354 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.358 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.337 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.328 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.505 |
LIG_SH3_4 | 499 | 506 | PF00018 | 0.252 |
LIG_SUMO_SIM_anti_2 | 332 | 338 | PF11976 | 0.539 |
LIG_SUMO_SIM_anti_2 | 404 | 410 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 128 | 133 | PF11976 | 0.529 |
LIG_WRC_WIRS_1 | 216 | 221 | PF05994 | 0.419 |
LIG_WRC_WIRS_1 | 312 | 317 | PF05994 | 0.432 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.665 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.461 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.552 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.401 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.285 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.718 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.701 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.290 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.419 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.290 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.259 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.295 |
MOD_Cter_Amidation | 287 | 290 | PF01082 | 0.419 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.609 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.635 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.602 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.388 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.663 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.290 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.312 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.321 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.746 |
MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.247 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.677 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.405 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.309 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.684 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.454 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.732 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.310 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.386 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.706 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.584 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.225 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.496 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.423 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.382 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.383 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.680 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.225 |
MOD_PK_1 | 128 | 134 | PF00069 | 0.524 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.516 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.208 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.458 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.308 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.225 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.283 |
MOD_Plk_2-3 | 320 | 326 | PF00069 | 0.421 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.214 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.487 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.396 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.492 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.474 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.555 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.208 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.390 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.532 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.504 |
MOD_SUMO_rev_2 | 430 | 440 | PF00179 | 0.208 |
TRG_DiLeu_BaEn_2 | 70 | 76 | PF01217 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 396 | 401 | PF01217 | 0.393 |
TRG_DiLeu_LyEn_5 | 237 | 242 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 592 | 594 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.521 |
TRG_NLS_MonoExtC_3 | 501 | 507 | PF00514 | 0.225 |
TRG_NLS_MonoExtN_4 | 499 | 506 | PF00514 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.474 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC92 | Leptomonas seymouri | 55% | 100% |
A0A1X0NRQ5 | Trypanosomatidae | 37% | 100% |
A0A3S7X4Q1 | Leishmania donovani | 75% | 100% |
A0A422N3Z8 | Trypanosoma rangeli | 35% | 100% |
A4I709 | Leishmania infantum | 75% | 100% |
C9ZWP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 95% |
E9B227 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q635 | Leishmania major | 74% | 100% |
V5AMB1 | Trypanosoma cruzi | 35% | 100% |