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: A0A3S7WS81
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 | 414 | 418 | PF00656 | 0.733 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.796 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.497 |
CLV_PCSK_FUR_1 | 173 | 177 | PF00082 | 0.624 |
CLV_PCSK_FUR_1 | 58 | 62 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.796 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 350 | 352 | PF00082 | 0.584 |
CLV_PCSK_PC7_1 | 21 | 27 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.539 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.634 |
DEG_SPOP_SBC_1 | 369 | 373 | PF00917 | 0.563 |
DOC_ANK_TNKS_1 | 145 | 152 | PF00023 | 0.649 |
DOC_CYCLIN_RxL_1 | 21 | 34 | PF00134 | 0.479 |
DOC_CYCLIN_RxL_1 | 4 | 12 | PF00134 | 0.393 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 297 | 305 | PF00069 | 0.590 |
DOC_PP4_FxxP_1 | 103 | 106 | PF00568 | 0.722 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.731 |
DOC_PP4_FxxP_1 | 464 | 467 | PF00568 | 0.632 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.827 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.761 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 181 | 189 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 244 | 254 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 323 | 328 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 332 | 341 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 460 | 467 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 488 | 496 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 93 | 103 | PF00244 | 0.569 |
LIG_AP2alpha_2 | 455 | 457 | PF02296 | 0.684 |
LIG_APCC_ABBA_1 | 29 | 34 | PF00400 | 0.393 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.746 |
LIG_eIF4E_1 | 24 | 30 | PF01652 | 0.411 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.758 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.523 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.664 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.584 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.728 |
LIG_GBD_Chelix_1 | 520 | 528 | PF00786 | 0.456 |
LIG_Integrin_RGD_1 | 474 | 476 | PF01839 | 0.648 |
LIG_LIR_Apic_2 | 188 | 192 | PF02991 | 0.731 |
LIG_LIR_Apic_2 | 324 | 330 | PF02991 | 0.601 |
LIG_LIR_Apic_2 | 462 | 467 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 67 | 74 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.561 |
LIG_PCNA_yPIPBox_3 | 525 | 538 | PF02747 | 0.483 |
LIG_RPA_C_Fungi | 233 | 245 | PF08784 | 0.555 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.411 |
LIG_SH2_SRC | 50 | 53 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.411 |
LIG_SH2_STAT3 | 277 | 280 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.498 |
LIG_SH3_1 | 585 | 591 | PF00018 | 0.616 |
LIG_SH3_2 | 197 | 202 | PF14604 | 0.595 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.644 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.680 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.661 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.715 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.726 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.769 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.698 |
LIG_TRAF2_1 | 598 | 601 | PF00917 | 0.567 |
MOD_CDC14_SPxK_1 | 347 | 350 | PF00782 | 0.565 |
MOD_CDK_SPK_2 | 544 | 549 | PF00069 | 0.508 |
MOD_CDK_SPxK_1 | 344 | 350 | PF00069 | 0.570 |
MOD_CDK_SPxxK_3 | 344 | 351 | PF00069 | 0.573 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.657 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.687 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.690 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.715 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.682 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.667 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.798 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.509 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.723 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.767 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.661 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.800 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.593 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.706 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.637 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.570 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.546 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.495 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.817 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.564 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.754 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.772 |
MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.736 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.661 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.678 |
MOD_GlcNHglycan | 311 | 315 | PF01048 | 0.482 |
MOD_GlcNHglycan | 417 | 421 | PF01048 | 0.769 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.590 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.696 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.571 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.760 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.459 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.792 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.548 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.688 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.705 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.716 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.717 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.424 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.725 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.715 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.752 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.687 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.645 |
MOD_N-GLC_2 | 160 | 162 | PF02516 | 0.780 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.658 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.734 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.611 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.699 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.644 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.572 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.597 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.609 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.774 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.643 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.692 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.623 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.607 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.604 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.601 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.641 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.658 |
MOD_PKB_1 | 236 | 244 | PF00069 | 0.679 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.641 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.697 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.626 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.526 |
MOD_Plk_2-3 | 150 | 156 | PF00069 | 0.667 |
MOD_Plk_2-3 | 252 | 258 | PF00069 | 0.810 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.786 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.588 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.612 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.688 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.736 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.616 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.733 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.489 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.673 |
MOD_SUMO_for_1 | 258 | 261 | PF00179 | 0.698 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.731 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 238 | 243 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 482 | 486 | PF00026 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 488 | 493 | PF00026 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 7 | 12 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC79 | Leptomonas seymouri | 36% | 100% |
A4H6Z1 | Leishmania braziliensis | 61% | 100% |
E9AGH2 | Leishmania infantum | 100% | 100% |
E9AP11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QGH8 | Leishmania major | 83% | 100% |