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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0031207 | Sec62/Sec63 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: E9B118
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006613 | cotranslational protein targeting to membrane | 6 | 1 |
GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 1 |
GO:0006620 | post-translational protein targeting to endoplasmic reticulum membrane | 6 | 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:0051668 | localization within membrane | 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 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0008320 | protein transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0022884 | macromolecule transmembrane transporter activity | 3 | 1 |
GO:0140318 | protein transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.752 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.764 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.754 |
DEG_APCC_DBOX_1 | 97 | 105 | PF00400 | 0.453 |
DEG_COP1_1 | 306 | 315 | PF00400 | 0.696 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.534 |
DEG_SPOP_SBC_1 | 127 | 131 | PF00917 | 0.542 |
DOC_ANK_TNKS_1 | 150 | 157 | PF00023 | 0.466 |
DOC_CYCLIN_RxL_1 | 193 | 206 | PF00134 | 0.443 |
DOC_CYCLIN_RxL_1 | 5 | 15 | PF00134 | 0.542 |
DOC_CYCLIN_RxL_1 | 59 | 67 | PF00134 | 0.362 |
DOC_MAPK_gen_1 | 282 | 289 | PF00069 | 0.669 |
DOC_MAPK_MEF2A_6 | 235 | 244 | PF00069 | 0.419 |
DOC_MAPK_RevD_3 | 238 | 251 | PF00069 | 0.451 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.489 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.557 |
DOC_USP7_UBL2_3 | 28 | 32 | PF12436 | 0.296 |
DOC_USP7_UBL2_3 | 62 | 66 | PF12436 | 0.362 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 260 | 269 | PF00244 | 0.525 |
LIG_Actin_WH2_2 | 50 | 68 | PF00022 | 0.296 |
LIG_AP2alpha_2 | 15 | 17 | PF02296 | 0.313 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.526 |
LIG_EVH1_2 | 315 | 319 | PF00568 | 0.736 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.423 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.479 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.334 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.649 |
LIG_LIR_Gen_1 | 165 | 176 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 327 | 334 | PF02991 | 0.726 |
LIG_LIR_Gen_1 | 67 | 78 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.389 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.480 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.714 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.743 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.296 |
LIG_SH2_NCK_1 | 330 | 334 | PF00017 | 0.743 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 330 | 334 | PF00017 | 0.729 |
LIG_SH2_STAT3 | 158 | 161 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.701 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.638 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.646 |
LIG_Sin3_3 | 293 | 300 | PF02671 | 0.621 |
LIG_TRAF2_1 | 135 | 138 | PF00917 | 0.476 |
LIG_TYR_ITIM | 318 | 323 | PF00017 | 0.684 |
LIG_WRC_WIRS_1 | 183 | 188 | PF05994 | 0.454 |
MOD_CDK_SPxxK_3 | 150 | 157 | PF00069 | 0.428 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.616 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.586 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.473 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.353 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.454 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.442 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.313 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.690 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.684 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.803 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.739 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.674 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.652 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.516 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.535 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.680 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.558 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.504 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.393 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.313 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.630 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.716 |
MOD_LATS_1 | 258 | 264 | PF00433 | 0.584 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.298 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.659 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.562 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.747 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.508 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.712 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.646 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.442 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.501 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.442 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.504 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.412 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.738 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.554 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.417 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.695 |
MOD_SUMO_for_1 | 192 | 195 | PF00179 | 0.432 |
MOD_SUMO_for_1 | 52 | 55 | PF00179 | 0.362 |
MOD_SUMO_rev_2 | 150 | 159 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 185 | 194 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 25 | 33 | PF00179 | 0.316 |
TRG_AP2beta_CARGO_1 | 15 | 24 | PF09066 | 0.296 |
TRG_DiLeu_BaLyEn_6 | 171 | 176 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 6 | 11 | PF01217 | 0.556 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.715 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.740 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.553 |
TRG_NLS_Bipartite_1 | 250 | 264 | PF00514 | 0.704 |
TRG_Pf-PMV_PEXEL_1 | 199 | 204 | PF00026 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 8 | 13 | PF00026 | 0.765 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCM1 | Leptomonas seymouri | 73% | 100% |
A0A0S4IL99 | Bodo saltans | 42% | 100% |
A0A1X0P2Q0 | Trypanosomatidae | 50% | 100% |
A0A3S7X3P0 | Leishmania donovani | 90% | 100% |
A4HIH6 | Leishmania braziliensis | 81% | 100% |
A4I5S3 | Leishmania infantum | 90% | 100% |
C9ZR42 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
Q4Q748 | Leishmania major | 92% | 100% |
V5AWW0 | Trypanosoma cruzi | 48% | 100% |