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: 9 |
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 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0031090 | organelle membrane | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AR93
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022406 | membrane docking | 2 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051643 | endoplasmic reticulum localization | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0061817 | endoplasmic reticulum-plasma membrane tethering | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090158 | endoplasmic reticulum membrane organization | 5 | 1 |
GO:0140056 | organelle localization by membrane tethering | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.376 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.781 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.768 |
DEG_SPOP_SBC_1 | 296 | 300 | PF00917 | 0.435 |
DOC_CYCLIN_yCln2_LP_2 | 133 | 139 | PF00134 | 0.534 |
DOC_MAPK_gen_1 | 126 | 133 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 262 | 270 | PF00069 | 0.265 |
DOC_MAPK_MEF2A_6 | 86 | 95 | PF00069 | 0.491 |
DOC_MAPK_RevD_3 | 268 | 284 | PF00069 | 0.216 |
DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.566 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.737 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 126 | 132 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 245 | 254 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 295 | 305 | PF00244 | 0.557 |
LIG_BIR_III_4 | 290 | 294 | PF00653 | 0.417 |
LIG_Clathr_ClatBox_1 | 42 | 46 | PF01394 | 0.407 |
LIG_EVH1_2 | 53 | 57 | PF00568 | 0.491 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.547 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.478 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.497 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.458 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.525 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.491 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.571 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.467 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.428 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.561 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.566 |
LIG_Integrin_RGD_1 | 155 | 157 | PF01839 | 0.453 |
LIG_LIR_Apic_2 | 181 | 185 | PF02991 | 0.646 |
LIG_LIR_Apic_2 | 373 | 378 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 102 | 111 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 147 | 154 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.419 |
LIG_MYND_1 | 141 | 145 | PF01753 | 0.643 |
LIG_NRBOX | 147 | 153 | PF00104 | 0.584 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 134 | 138 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 375 | 379 | PF00017 | 0.413 |
LIG_SH2_PTP2 | 187 | 190 | PF00017 | 0.596 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.468 |
LIG_SH2_SRC | 187 | 190 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.491 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.606 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.604 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.529 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.544 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.549 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.491 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.491 |
LIG_SUMO_SIM_anti_2 | 277 | 282 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 135 | 140 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 272 | 277 | PF11976 | 0.310 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.550 |
LIG_TRFH_1 | 26 | 30 | PF08558 | 0.600 |
LIG_WRC_WIRS_1 | 179 | 184 | PF05994 | 0.645 |
LIG_WW_1 | 184 | 187 | PF00397 | 0.582 |
MOD_CDC14_SPxK_1 | 29 | 32 | PF00782 | 0.599 |
MOD_CDK_SPK_2 | 141 | 146 | PF00069 | 0.563 |
MOD_CDK_SPxK_1 | 26 | 32 | PF00069 | 0.598 |
MOD_CDK_SPxxK_3 | 26 | 33 | PF00069 | 0.600 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.604 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.653 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.740 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.663 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.506 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.425 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.533 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.518 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.760 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.506 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.606 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.558 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.810 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.294 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.649 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.725 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.688 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.573 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.476 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.578 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.302 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.538 |
MOD_NEK2_2 | 178 | 183 | PF00069 | 0.642 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.600 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.532 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.519 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.425 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.573 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.573 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.531 |
MOD_PKB_1 | 243 | 251 | PF00069 | 0.573 |
MOD_Plk_2-3 | 135 | 141 | PF00069 | 0.542 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.634 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.612 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.571 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.721 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.672 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.598 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.591 |
MOD_SUMO_for_1 | 43 | 46 | PF00179 | 0.491 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.473 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.596 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILZ1 | Leptomonas seymouri | 49% | 100% |
A0A3S5H717 | Leishmania donovani | 76% | 95% |
A4H978 | Leishmania braziliensis | 61% | 96% |
A4HXJ8 | Leishmania infantum | 76% | 95% |
Q4QE70 | Leishmania major | 75% | 100% |