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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q635
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043171 | peptide catabolic process | 4 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004177 | aminopeptidase activity | 5 | 9 |
GO:0005488 | binding | 1 | 10 |
GO:0008233 | peptidase activity | 3 | 10 |
GO:0008235 | metalloexopeptidase activity | 5 | 2 |
GO:0008237 | metallopeptidase activity | 4 | 10 |
GO:0008238 | exopeptidase activity | 4 | 9 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0033218 | amide binding | 2 | 2 |
GO:0042277 | peptide binding | 3 | 2 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0070006 | metalloaminopeptidase activity | 6 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.672 |
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.485 |
CLV_PCSK_FUR_1 | 110 | 114 | PF00082 | 0.539 |
CLV_PCSK_FUR_1 | 74 | 78 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.759 |
CLV_PCSK_PC7_1 | 400 | 406 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.344 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.587 |
DEG_SPOP_SBC_1 | 550 | 554 | PF00917 | 0.468 |
DEG_SPOP_SBC_1 | 555 | 559 | PF00917 | 0.405 |
DOC_CYCLIN_RxL_1 | 413 | 423 | PF00134 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 510 | 516 | PF00134 | 0.312 |
DOC_MAPK_MEF2A_6 | 605 | 614 | PF00069 | 0.402 |
DOC_PP1_RVXF_1 | 220 | 227 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 293 | 299 | PF00149 | 0.434 |
DOC_PP2B_LxvP_1 | 510 | 513 | PF13499 | 0.312 |
DOC_PP2B_PxIxI_1 | 614 | 620 | PF00149 | 0.507 |
DOC_PP4_FxxP_1 | 286 | 289 | PF00568 | 0.344 |
DOC_PP4_FxxP_1 | 432 | 435 | PF00568 | 0.344 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.740 |
DOC_USP7_MATH_2 | 98 | 104 | PF00917 | 0.529 |
DOC_USP7_UBL2_3 | 187 | 191 | PF12436 | 0.635 |
DOC_USP7_UBL2_3 | 531 | 535 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.708 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 408 | 417 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 568 | 576 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 629 | 639 | PF00244 | 0.557 |
LIG_Actin_WH2_2 | 146 | 163 | PF00022 | 0.384 |
LIG_Clathr_ClatBox_1 | 223 | 227 | PF01394 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 218 | 226 | PF00928 | 0.493 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.660 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.484 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.592 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.562 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.412 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.440 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.409 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.461 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.777 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.344 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.443 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.361 |
LIG_LIR_Gen_1 | 103 | 109 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 346 | 354 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 393 | 402 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 346 | 350 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.504 |
LIG_NRBOX | 443 | 449 | PF00104 | 0.484 |
LIG_PDZ_Class_1 | 649 | 654 | PF00595 | 0.589 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.484 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 394 | 398 | PF00017 | 0.444 |
LIG_SH2_SRC | 471 | 474 | PF00017 | 0.402 |
LIG_SH2_SRC | 581 | 584 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 105 | 109 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.412 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.395 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.369 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.471 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.379 |
LIG_SH3_3 | 609 | 615 | PF00018 | 0.521 |
LIG_SH3_3 | 632 | 638 | PF00018 | 0.604 |
LIG_SUMO_SIM_anti_2 | 363 | 370 | PF11976 | 0.573 |
LIG_SUMO_SIM_anti_2 | 442 | 448 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 137 | 143 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 161 | 166 | PF11976 | 0.534 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.555 |
LIG_TRFH_1 | 394 | 398 | PF08558 | 0.444 |
LIG_TYR_ITIM | 392 | 397 | PF00017 | 0.449 |
LIG_WRC_WIRS_1 | 248 | 253 | PF05994 | 0.443 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.452 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.583 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.760 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.685 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.356 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.604 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.561 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.477 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.394 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.699 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.344 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.443 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.324 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.361 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.634 |
MOD_Cter_Amidation | 319 | 322 | PF01082 | 0.443 |
MOD_Cter_Amidation | 473 | 476 | PF01082 | 0.428 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.545 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.635 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.719 |
MOD_GlcNHglycan | 227 | 231 | PF01048 | 0.258 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.688 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.602 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.324 |
MOD_GlcNHglycan | 543 | 547 | PF01048 | 0.371 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.509 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.454 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.406 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.575 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.737 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.749 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.693 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.699 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.446 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.366 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.561 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.411 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.539 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.334 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.344 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.188 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.680 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.718 |
MOD_N-GLC_1 | 390 | 395 | PF02516 | 0.525 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.574 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.622 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.651 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.653 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.536 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.448 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.402 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.402 |
MOD_PK_1 | 161 | 167 | PF00069 | 0.530 |
MOD_PKA_1 | 186 | 192 | PF00069 | 0.704 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.484 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.484 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.512 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.440 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.621 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.481 |
MOD_Plk_2-3 | 100 | 106 | PF00069 | 0.617 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.448 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.406 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.518 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.709 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.416 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.498 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.440 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.636 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.710 |
MOD_SUMO_for_1 | 354 | 357 | PF00179 | 0.561 |
TRG_DiLeu_BaEn_1 | 492 | 497 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_2 | 103 | 109 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_4 | 620 | 626 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.443 |
TRG_DiLeu_LyEn_5 | 269 | 274 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.471 |
TRG_NLS_MonoExtN_4 | 191 | 197 | PF00514 | 0.615 |
TRG_NLS_MonoExtN_4 | 319 | 325 | PF00514 | 0.258 |
TRG_Pf-PMV_PEXEL_1 | 113 | 117 | PF00026 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 137 | 142 | PF00026 | 0.373 |
TRG_Pf-PMV_PEXEL_1 | 586 | 590 | PF00026 | 0.258 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC92 | Leptomonas seymouri | 56% | 100% |
A0A3S7X4Q1 | Leishmania donovani | 92% | 100% |
A0A422N3Z8 | Trypanosoma rangeli | 36% | 100% |
A4HJK9 | Leishmania braziliensis | 74% | 100% |
A4I709 | Leishmania infantum | 92% | 100% |
C9ZWP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B227 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5AMB1 | Trypanosoma cruzi | 35% | 100% |