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: A0A3S7X4Q1
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 | 49 | 53 | PF00656 | 0.617 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.506 |
CLV_PCSK_FUR_1 | 41 | 45 | PF00082 | 0.555 |
CLV_PCSK_FUR_1 | 77 | 81 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.743 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.364 |
CLV_PCSK_PC7_1 | 367 | 373 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.505 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.523 |
DEG_SPOP_SBC_1 | 323 | 327 | PF00917 | 0.689 |
DEG_SPOP_SBC_1 | 517 | 521 | PF00917 | 0.433 |
DEG_SPOP_SBC_1 | 522 | 526 | PF00917 | 0.368 |
DOC_CYCLIN_RxL_1 | 380 | 390 | PF00134 | 0.494 |
DOC_MAPK_MEF2A_6 | 572 | 581 | PF00069 | 0.396 |
DOC_PP1_RVXF_1 | 187 | 194 | PF00149 | 0.401 |
DOC_PP1_RVXF_1 | 260 | 266 | PF00149 | 0.410 |
DOC_PP2B_PxIxI_1 | 581 | 587 | PF00149 | 0.490 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.465 |
DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.335 |
DOC_PP4_FxxP_1 | 399 | 402 | PF00568 | 0.335 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.713 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.636 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 375 | 384 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 535 | 543 | PF00244 | 0.396 |
LIG_APCC_ABBA_1 | 199 | 204 | PF00400 | 0.524 |
LIG_Clathr_ClatBox_1 | 190 | 194 | PF01394 | 0.498 |
LIG_deltaCOP1_diTrp_1 | 185 | 193 | PF00928 | 0.494 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.414 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.288 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.463 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.471 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.585 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.521 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.443 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.390 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.771 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.335 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.447 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.355 |
LIG_LIR_Gen_1 | 313 | 321 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 360 | 369 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 70 | 76 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 360 | 364 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.530 |
LIG_NRBOX | 410 | 416 | PF00104 | 0.479 |
LIG_PDZ_Class_1 | 616 | 621 | PF00595 | 0.608 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.479 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.525 |
LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.518 |
LIG_SH2_SRC | 438 | 441 | PF00017 | 0.396 |
LIG_SH2_SRC | 548 | 551 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.404 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.378 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.340 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.468 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.373 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.252 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.523 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.575 |
LIG_SUMO_SIM_anti_2 | 331 | 337 | PF11976 | 0.563 |
LIG_SUMO_SIM_anti_2 | 409 | 415 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 104 | 110 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 128 | 133 | PF11976 | 0.554 |
LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.541 |
LIG_TRFH_1 | 361 | 365 | PF08558 | 0.439 |
LIG_TYR_ITIM | 359 | 364 | PF00017 | 0.446 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.447 |
LIG_WRC_WIRS_1 | 311 | 316 | PF05994 | 0.459 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.610 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.749 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.678 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.565 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.340 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.601 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.434 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.330 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.685 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.335 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.447 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.319 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.476 |
MOD_Cter_Amidation | 286 | 289 | PF01082 | 0.447 |
MOD_Cter_Amidation | 440 | 443 | PF01082 | 0.432 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.564 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.650 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.690 |
MOD_GlcNHglycan | 2 | 6 | PF01048 | 0.614 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.518 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.419 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.689 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.608 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.319 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.362 |
MOD_GlcNHglycan | 510 | 514 | PF01048 | 0.357 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.718 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.495 |
MOD_GlcNHglycan | 587 | 591 | PF01048 | 0.406 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.609 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.702 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.542 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.702 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.420 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.355 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.696 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.597 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.378 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.326 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.335 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.179 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.701 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.527 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.455 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.558 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.490 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.487 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.396 |
MOD_PK_1 | 128 | 134 | PF00069 | 0.551 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.687 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.520 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.479 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.621 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.444 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.539 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.483 |
MOD_Plk_2-3 | 67 | 73 | PF00069 | 0.596 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.521 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.511 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.392 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.495 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.422 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.406 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.577 |
MOD_SUMO_for_1 | 321 | 324 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_1 | 459 | 464 | PF01217 | 0.387 |
TRG_DiLeu_BaEn_2 | 70 | 76 | PF01217 | 0.557 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.428 |
TRG_DiLeu_LyEn_5 | 236 | 241 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.555 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC92 | Leptomonas seymouri | 57% | 100% |
A0A1X0NRQ5 | Trypanosomatidae | 38% | 100% |
A0A422N3Z8 | Trypanosoma rangeli | 35% | 100% |
A4HJK9 | Leishmania braziliensis | 75% | 99% |
A4I709 | Leishmania infantum | 100% | 100% |
C9ZWP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 96% |
E9B227 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q635 | Leishmania major | 92% | 100% |
V5AMB1 | Trypanosoma cruzi | 35% | 100% |