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: 5 |
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 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A0A3S7WQ88
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.519 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.575 |
DEG_SCF_FBW7_2 | 55 | 61 | PF00400 | 0.374 |
DOC_CKS1_1 | 192 | 197 | PF01111 | 0.424 |
DOC_CKS1_1 | 210 | 215 | PF01111 | 0.353 |
DOC_CKS1_1 | 55 | 60 | PF01111 | 0.375 |
DOC_CYCLIN_RxL_1 | 175 | 186 | PF00134 | 0.478 |
DOC_MAPK_gen_1 | 67 | 78 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 71 | 80 | PF00069 | 0.377 |
DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.435 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.421 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.354 |
DOC_USP7_UBL2_3 | 67 | 71 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.369 |
LIG_14-3-3_CanoR_1 | 111 | 115 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 12 | 16 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 277 | 284 | PF00244 | 0.657 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.599 |
LIG_deltaCOP1_diTrp_1 | 249 | 255 | PF00928 | 0.408 |
LIG_EH_1 | 230 | 234 | PF12763 | 0.377 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.453 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.481 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.546 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.505 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.461 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.253 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.416 |
LIG_LIR_Apic_2 | 191 | 195 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 208 | 213 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 253 | 262 | PF02991 | 0.302 |
LIG_LIR_LC3C_4 | 268 | 272 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.328 |
LIG_PTB_Apo_2 | 239 | 246 | PF02174 | 0.356 |
LIG_SH2_GRB2like | 146 | 149 | PF00017 | 0.382 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.382 |
LIG_SUMO_SIM_anti_2 | 268 | 275 | PF11976 | 0.452 |
LIG_SUMO_SIM_anti_2 | 286 | 293 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 6 | 14 | PF11976 | 0.585 |
LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.472 |
MOD_CDK_SPxxK_3 | 209 | 216 | PF00069 | 0.444 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.679 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.480 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.729 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.354 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.413 |
MOD_Cter_Amidation | 275 | 278 | PF01082 | 0.412 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.677 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.429 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.525 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.592 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.364 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.386 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.525 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.674 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.640 |
MOD_N-GLC_2 | 149 | 151 | PF02516 | 0.627 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.635 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.568 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.464 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.479 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.460 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.232 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.262 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.339 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.551 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.323 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.448 |
MOD_NEK2_2 | 236 | 241 | PF00069 | 0.463 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.462 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.332 |
MOD_PKA_1 | 183 | 189 | PF00069 | 0.423 |
MOD_PKA_1 | 277 | 283 | PF00069 | 0.676 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.530 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.615 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.448 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.665 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.435 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.505 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.372 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.356 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.321 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.585 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.290 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.314 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.527 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.400 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.370 |
TRG_DiLeu_BaEn_1 | 295 | 300 | PF01217 | 0.685 |
TRG_DiLeu_LyEn_5 | 295 | 300 | PF01217 | 0.738 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.676 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I287 | Leptomonas seymouri | 40% | 100% |
A4H5G2 | Leishmania braziliensis | 58% | 98% |
A4HTL2 | Leishmania infantum | 100% | 100% |
E9AME3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QIA5 | Leishmania major | 82% | 100% |