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:0005789 | endoplasmic reticulum membrane | 4 | 6 |
GO:0016020 | membrane | 2 | 7 |
GO:0031090 | organelle membrane | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005785 | signal recognition particle receptor complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HLX3
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0045047 | protein targeting to ER | 6 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005525 | GTP binding | 5 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0019001 | guanyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003746 | translation elongation factor activity | 4 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 1 |
GO:0045182 | translation regulator activity | 1 | 1 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 317 | 321 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.642 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.612 |
CLV_Separin_Metazoa | 298 | 302 | PF03568 | 0.438 |
DEG_SPOP_SBC_1 | 228 | 232 | PF00917 | 0.619 |
DOC_ANK_TNKS_1 | 401 | 408 | PF00023 | 0.665 |
DOC_ANK_TNKS_1 | 67 | 74 | PF00023 | 0.462 |
DOC_CYCLIN_RxL_1 | 250 | 258 | PF00134 | 0.438 |
DOC_CYCLIN_RxL_1 | 344 | 353 | PF00134 | 0.546 |
DOC_CYCLIN_RxL_1 | 364 | 371 | PF00134 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 457 | 463 | PF00134 | 0.620 |
DOC_MAPK_gen_1 | 225 | 235 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 416 | 422 | PF00069 | 0.774 |
DOC_MAPK_MEF2A_6 | 229 | 237 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 242 | 249 | PF00069 | 0.564 |
DOC_PP1_RVXF_1 | 213 | 220 | PF00149 | 0.576 |
DOC_PP1_RVXF_1 | 344 | 351 | PF00149 | 0.549 |
DOC_PP2B_LxvP_1 | 30 | 33 | PF13499 | 0.458 |
DOC_PP2B_LxvP_1 | 457 | 460 | PF13499 | 0.630 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.463 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.732 |
DOC_USP7_MATH_2 | 40 | 46 | PF00917 | 0.414 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 226 | 235 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 259 | 263 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 301 | 310 | PF00244 | 0.466 |
LIG_Actin_WH2_2 | 428 | 444 | PF00022 | 0.647 |
LIG_Actin_WH2_2 | 44 | 61 | PF00022 | 0.397 |
LIG_APCC_ABBAyCdc20_2 | 417 | 423 | PF00400 | 0.592 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.531 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.261 |
LIG_BRCT_BRCA1_1 | 338 | 342 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 450 | 454 | PF00533 | 0.714 |
LIG_deltaCOP1_diTrp_1 | 194 | 197 | PF00928 | 0.419 |
LIG_EH1_1 | 342 | 350 | PF00400 | 0.546 |
LIG_eIF4E_1 | 343 | 349 | PF01652 | 0.546 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.506 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.513 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.549 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.528 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.619 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.546 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.590 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.503 |
LIG_GBD_Chelix_1 | 329 | 337 | PF00786 | 0.346 |
LIG_HCF-1_HBM_1 | 474 | 477 | PF13415 | 0.657 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 243 | 250 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.644 |
LIG_MAD2 | 285 | 293 | PF02301 | 0.619 |
LIG_NRBOX | 328 | 334 | PF00104 | 0.520 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.597 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.546 |
LIG_SUMO_SIM_anti_2 | 478 | 484 | PF11976 | 0.688 |
LIG_SUMO_SIM_par_1 | 308 | 315 | PF11976 | 0.546 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.389 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.438 |
LIG_TYR_ITIM | 204 | 209 | PF00017 | 0.411 |
LIG_UBA3_1 | 234 | 242 | PF00899 | 0.546 |
LIG_WRC_WIRS_1 | 187 | 192 | PF05994 | 0.526 |
LIG_WRC_WIRS_1 | 208 | 213 | PF05994 | 0.261 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.419 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.460 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.472 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.546 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.592 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.546 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.546 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.739 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.573 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.424 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.517 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.550 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.502 |
MOD_Cter_Amidation | 407 | 410 | PF01082 | 0.564 |
MOD_Cter_Amidation | 414 | 417 | PF01082 | 0.566 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.694 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.759 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.641 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.346 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.406 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.567 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.483 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.499 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.698 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.238 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.704 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.513 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.364 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.506 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.552 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.454 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.389 |
MOD_PK_1 | 134 | 140 | PF00069 | 0.413 |
MOD_PK_1 | 387 | 393 | PF00069 | 0.535 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.552 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.555 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.406 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.483 |
MOD_PKB_1 | 225 | 233 | PF00069 | 0.648 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.400 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.438 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.558 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.502 |
MOD_Plk_2-3 | 314 | 320 | PF00069 | 0.546 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.489 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.444 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.444 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.458 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.364 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.546 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.521 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.460 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.409 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.517 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.546 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.485 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.567 |
MOD_SUMO_rev_2 | 468 | 478 | PF00179 | 0.661 |
TRG_DiLeu_BaEn_1 | 194 | 199 | PF01217 | 0.238 |
TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.655 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.238 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2X6 | Leptomonas seymouri | 50% | 100% |
A0A3S7X750 | Leishmania donovani | 69% | 100% |
A4I9A2 | Leishmania infantum | 69% | 100% |
E9B4A2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4Q3S4 | Leishmania major | 69% | 100% |