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:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4I4H6
Term | Name | Level | Count |
---|---|---|---|
GO:0006914 | autophagy | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016236 | macroautophagy | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.632 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.509 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.483 |
DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.444 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.694 |
DOC_AGCK_PIF_2 | 465 | 470 | PF00069 | 0.386 |
DOC_CKS1_1 | 450 | 455 | PF01111 | 0.312 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 125 | 134 | PF00134 | 0.529 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.615 |
DOC_MAPK_gen_1 | 37 | 46 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 574 | 582 | PF00069 | 0.388 |
DOC_MAPK_RevD_3 | 25 | 39 | PF00069 | 0.678 |
DOC_PP2B_LxvP_1 | 582 | 585 | PF13499 | 0.312 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.661 |
DOC_PP4_FxxP_1 | 53 | 56 | PF00568 | 0.640 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.700 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 187 | 197 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 323 | 332 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 345 | 352 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 353 | 360 | PF00244 | 0.647 |
LIG_Actin_WH2_2 | 195 | 212 | PF00022 | 0.388 |
LIG_Actin_WH2_2 | 322 | 340 | PF00022 | 0.664 |
LIG_AP2alpha_2 | 412 | 414 | PF02296 | 0.703 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.340 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.558 |
LIG_CtBP_PxDLS_1 | 2 | 6 | PF00389 | 0.705 |
LIG_deltaCOP1_diTrp_1 | 235 | 243 | PF00928 | 0.587 |
LIG_eIF4E_1 | 233 | 239 | PF01652 | 0.561 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.340 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.746 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.572 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.618 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.581 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.630 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.639 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.567 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.679 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.426 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.779 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.703 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.662 |
LIG_GBD_Chelix_1 | 576 | 584 | PF00786 | 0.340 |
LIG_LIR_Apic_2 | 107 | 111 | PF02991 | 0.668 |
LIG_LIR_Apic_2 | 540 | 545 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 112 | 120 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 192 | 202 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 412 | 421 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 534 | 543 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.183 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 534 | 538 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 556 | 562 | PF02991 | 0.569 |
LIG_NRBOX | 121 | 127 | PF00104 | 0.602 |
LIG_NRBOX | 192 | 198 | PF00104 | 0.388 |
LIG_PALB2_WD40_1 | 224 | 232 | PF16756 | 0.388 |
LIG_PDZ_Class_1 | 592 | 597 | PF00595 | 0.578 |
LIG_Pex14_1 | 207 | 211 | PF04695 | 0.398 |
LIG_Pex14_2 | 555 | 559 | PF04695 | 0.558 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.312 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 533 | 537 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 560 | 564 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 569 | 573 | PF00017 | 0.604 |
LIG_SH2_STAT3 | 211 | 214 | PF00017 | 0.397 |
LIG_SH2_STAT3 | 472 | 475 | PF00017 | 0.572 |
LIG_SH2_STAT3 | 533 | 536 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.312 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.715 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.578 |
LIG_SUMO_SIM_anti_2 | 326 | 334 | PF11976 | 0.678 |
LIG_SUMO_SIM_par_1 | 1 | 8 | PF11976 | 0.667 |
LIG_SUMO_SIM_par_1 | 195 | 201 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 26 | 32 | PF11976 | 0.686 |
LIG_TYR_ITIM | 141 | 146 | PF00017 | 0.312 |
LIG_TYR_ITIM | 581 | 586 | PF00017 | 0.304 |
LIG_WRC_WIRS_1 | 22 | 27 | PF05994 | 0.595 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.487 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.308 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.621 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.315 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.681 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.667 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.591 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.576 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.753 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.676 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.312 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.375 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.468 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.515 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.490 |
MOD_GlcNHglycan | 309 | 313 | PF01048 | 0.482 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.501 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.535 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.478 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.502 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.392 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.332 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.340 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.501 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.519 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.460 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.740 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.443 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.408 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.725 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.429 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.780 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.726 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.696 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.704 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.737 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.342 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.319 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.773 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.479 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.561 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.313 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.407 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.304 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.732 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.657 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.674 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.285 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.712 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.344 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.608 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.799 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.291 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.737 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.734 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.674 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.561 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.643 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.643 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.603 |
MOD_Plk_2-3 | 316 | 322 | PF00069 | 0.642 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.768 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.388 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.388 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.388 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.298 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.561 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.643 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.640 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.657 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.604 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.235 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.312 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.312 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.436 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.770 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.736 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.636 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.312 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.715 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.711 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.710 |
MOD_SUMO_rev_2 | 114 | 122 | PF00179 | 0.574 |
TRG_DiLeu_LyEn_5 | 445 | 450 | PF01217 | 0.329 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 38 | 41 | PF00400 | 0.695 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR7 | Leptomonas seymouri | 50% | 100% |
A0A3S7X2B9 | Leishmania donovani | 99% | 100% |
A4HHD1 | Leishmania braziliensis | 84% | 100% |
E9ADX7 | Leishmania major | 94% | 100% |
E9ALV4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |