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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AP11
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0006458 | 'de novo' protein folding | 3 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0010243 | response to organonitrogen compound | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0035966 | response to topologically incorrect protein | 3 | 1 |
GO:0035967 | cellular response to topologically incorrect protein | 4 | 1 |
GO:0036503 | ERAD pathway | 5 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 1 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0051788 | response to misfolded protein | 4 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
GO:0070887 | cellular response to chemical stimulus | 3 | 1 |
GO:0071218 | cellular response to misfolded protein | 5 | 1 |
GO:0071310 | cellular response to organic substance | 4 | 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 |
GO:1901698 | response to nitrogen compound | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0030544 | Hsp70 protein binding | 4 | 1 |
GO:0031072 | heat shock protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.632 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.376 |
CLV_PCSK_FUR_1 | 173 | 177 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.259 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.312 |
DEG_APCC_DBOX_1 | 580 | 588 | PF00400 | 0.454 |
DEG_SPOP_SBC_1 | 588 | 592 | PF00917 | 0.587 |
DOC_ANK_TNKS_1 | 145 | 152 | PF00023 | 0.594 |
DOC_CKS1_1 | 229 | 234 | PF01111 | 0.491 |
DOC_CYCLIN_RxL_1 | 4 | 12 | PF00134 | 0.292 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 296 | 304 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 331 | 340 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.211 |
DOC_PP4_FxxP_1 | 103 | 106 | PF00568 | 0.611 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.628 |
DOC_PP4_FxxP_1 | 212 | 215 | PF00568 | 0.498 |
DOC_PP4_FxxP_1 | 460 | 463 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.691 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 181 | 189 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 350 | 359 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 484 | 493 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 581 | 585 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 615 | 619 | PF00244 | 0.712 |
LIG_APCC_ABBA_1 | 29 | 34 | PF00400 | 0.309 |
LIG_BIR_III_2 | 451 | 455 | PF00653 | 0.504 |
LIG_BRCT_BRCA1_1 | 203 | 207 | PF00533 | 0.696 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.654 |
LIG_CSL_BTD_1 | 244 | 247 | PF09270 | 0.512 |
LIG_eIF4E_1 | 24 | 30 | PF01652 | 0.308 |
LIG_EVH1_1 | 584 | 588 | PF00568 | 0.479 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.659 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.505 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.703 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.379 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.595 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.530 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.660 |
LIG_GBD_Chelix_1 | 516 | 524 | PF00786 | 0.399 |
LIG_LIR_Apic_2 | 188 | 192 | PF02991 | 0.628 |
LIG_LIR_Apic_2 | 209 | 215 | PF02991 | 0.504 |
LIG_LIR_Apic_2 | 323 | 329 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 458 | 463 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.556 |
LIG_MYND_1 | 585 | 589 | PF01753 | 0.484 |
LIG_Rb_LxCxE_1 | 637 | 646 | PF01857 | 0.458 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.308 |
LIG_SH2_CRK | 630 | 634 | PF00017 | 0.478 |
LIG_SH2_NCK_1 | 326 | 330 | PF00017 | 0.528 |
LIG_SH2_SRC | 50 | 53 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.331 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.633 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.599 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.563 |
LIG_SH3_3 | 630 | 636 | PF00018 | 0.513 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.614 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.630 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.591 |
LIG_WW_2 | 585 | 588 | PF00397 | 0.486 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.587 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.679 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.667 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.597 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.573 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.663 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.510 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.511 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.546 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.554 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.593 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.619 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.628 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.581 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.766 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.642 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.684 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.444 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.426 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.395 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.781 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.537 |
MOD_GlcNHglycan | 141 | 145 | PF01048 | 0.706 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.765 |
MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.616 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.673 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.613 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.564 |
MOD_GlcNHglycan | 310 | 314 | PF01048 | 0.663 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.565 |
MOD_GlcNHglycan | 413 | 417 | PF01048 | 0.709 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.564 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.493 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.687 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.452 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.430 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.533 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.680 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.538 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.551 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.697 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.693 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.603 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.626 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.628 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.636 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.620 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.386 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.685 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.555 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.497 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.654 |
MOD_N-GLC_2 | 160 | 162 | PF02516 | 0.665 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.682 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.655 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.711 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.608 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.345 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.494 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.480 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.423 |
MOD_NEK2_1 | 618 | 623 | PF00069 | 0.649 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.691 |
MOD_PK_1 | 280 | 286 | PF00069 | 0.532 |
MOD_PK_1 | 634 | 640 | PF00069 | 0.530 |
MOD_PKA_1 | 280 | 286 | PF00069 | 0.532 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.706 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.596 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.557 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.524 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.528 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.538 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.522 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.444 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.693 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.548 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.349 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.422 |
MOD_Plk_2-3 | 251 | 257 | PF00069 | 0.696 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.516 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.565 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.506 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.498 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.572 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.664 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.497 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.472 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.530 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.600 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.571 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.573 |
MOD_SUMO_rev_2 | 17 | 23 | PF00179 | 0.262 |
MOD_SUMO_rev_2 | 251 | 260 | PF00179 | 0.527 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.193 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.551 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 478 | 482 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 7 | 12 | PF00026 | 0.337 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC79 | Leptomonas seymouri | 37% | 100% |
A0A3S7WS81 | Leishmania donovani | 78% | 100% |
A4H6Z1 | Leishmania braziliensis | 61% | 100% |
E9AGH2 | Leishmania infantum | 78% | 100% |
Q4QGH8 | Leishmania major | 75% | 100% |