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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9B070
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.844 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.759 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.759 |
DEG_SPOP_SBC_1 | 170 | 174 | PF00917 | 0.435 |
DOC_MAPK_MEF2A_6 | 295 | 303 | PF00069 | 0.593 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.480 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 119 | 128 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 9 | 17 | PF00244 | 0.611 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.238 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.638 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.567 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.505 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.473 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.491 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.367 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.624 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.745 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.551 |
LIG_Integrin_isoDGR_2 | 43 | 45 | PF01839 | 0.755 |
LIG_LIR_Apic_2 | 82 | 88 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.598 |
LIG_PDZ_Class_2 | 298 | 303 | PF00595 | 0.784 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.324 |
LIG_PTB_Apo_2 | 86 | 93 | PF02174 | 0.420 |
LIG_PTB_Phospho_1 | 86 | 92 | PF10480 | 0.422 |
LIG_SH2_NCK_1 | 85 | 89 | PF00017 | 0.488 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.452 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.752 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.471 |
LIG_UBA3_1 | 163 | 169 | PF00899 | 0.468 |
LIG_WRC_WIRS_1 | 240 | 245 | PF05994 | 0.523 |
MOD_CDK_SPK_2 | 79 | 84 | PF00069 | 0.421 |
MOD_CDK_SPxxK_3 | 181 | 188 | PF00069 | 0.494 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.485 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.646 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.487 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.578 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.549 |
MOD_Cter_Amidation | 43 | 46 | PF01082 | 0.755 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.473 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.629 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.625 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.794 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.721 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.579 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.566 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.293 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.772 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.709 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.587 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.576 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.575 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.333 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.535 |
MOD_LATS_1 | 117 | 123 | PF00433 | 0.431 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.742 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.303 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.530 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.802 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.609 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.534 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.802 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.413 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.259 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.447 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.572 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.517 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.500 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.514 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.477 |
MOD_SUMO_for_1 | 83 | 86 | PF00179 | 0.503 |
TRG_DiLeu_LyEn_5 | 159 | 164 | PF01217 | 0.417 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.597 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.756 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X1W1 | Leishmania donovani | 77% | 100% |
A4HGV0 | Leishmania braziliensis | 56% | 100% |
A4I3Y0 | Leishmania infantum | 77% | 100% |
Q4Q815 | Leishmania major | 74% | 100% |