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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 24 |
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 | yes | yes: 15, no: 2 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: A0A3S5H4S6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.704 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.641 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.666 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.729 |
DEG_APCC_DBOX_1 | 1 | 9 | PF00400 | 0.351 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.475 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.506 |
DEG_SPOP_SBC_1 | 59 | 63 | PF00917 | 0.345 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.437 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.345 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 133 | 141 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.741 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.477 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.369 |
LIG_deltaCOP1_diTrp_1 | 100 | 108 | PF00928 | 0.441 |
LIG_eIF4E_1 | 157 | 163 | PF01652 | 0.492 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.494 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.463 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.421 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.563 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.440 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.790 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.470 |
LIG_GBD_Chelix_1 | 251 | 259 | PF00786 | 0.512 |
LIG_IRF3_LxIS_1 | 258 | 265 | PF10401 | 0.351 |
LIG_LIR_Apic_2 | 232 | 237 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 177 | 188 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 45 | 55 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.384 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.508 |
LIG_SH2_GRB2like | 141 | 144 | PF00017 | 0.413 |
LIG_SH2_GRB2like | 290 | 293 | PF00017 | 0.875 |
LIG_SH2_PTP2 | 256 | 259 | PF00017 | 0.379 |
LIG_SH2_SRC | 188 | 191 | PF00017 | 0.540 |
LIG_SH2_SRC | 319 | 322 | PF00017 | 0.669 |
LIG_SH2_STAP1 | 25 | 29 | PF00017 | 0.381 |
LIG_SH2_STAT3 | 290 | 293 | PF00017 | 0.717 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.487 |
LIG_SH3_1 | 198 | 204 | PF00018 | 0.475 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.457 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.548 |
LIG_SUMO_SIM_par_1 | 42 | 47 | PF11976 | 0.325 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.429 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.468 |
LIG_TYR_ITIM | 254 | 259 | PF00017 | 0.486 |
MOD_CDK_SPxxK_3 | 126 | 133 | PF00069 | 0.429 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.545 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.443 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.498 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.747 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.844 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.417 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.472 |
MOD_Cter_Amidation | 158 | 161 | PF01082 | 0.694 |
MOD_Cter_Amidation | 222 | 225 | PF01082 | 0.636 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.724 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.639 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.823 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.635 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.625 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.641 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.674 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.557 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.503 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.425 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.582 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.739 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.782 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.401 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.745 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.779 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.457 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.461 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.573 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.717 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.700 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.375 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.577 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.755 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.720 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.447 |
MOD_PK_1 | 311 | 317 | PF00069 | 0.707 |
MOD_PKA_1 | 306 | 312 | PF00069 | 0.749 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.414 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.415 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.724 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.536 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.522 |
MOD_Plk_2-3 | 321 | 327 | PF00069 | 0.813 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.505 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.363 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.763 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.452 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.472 |
TRG_ER_diArg_1 | 272 | 275 | PF00400 | 0.746 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.839 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P471 | Leptomonas seymouri | 38% | 100% |
A0A0N1I022 | Leptomonas seymouri | 49% | 98% |
A0A1X0NWG7 | Trypanosomatidae | 24% | 91% |
A0A1X0NWG9 | Trypanosomatidae | 25% | 92% |
A0A1X0NXT1 | Trypanosomatidae | 24% | 92% |
A0A1X0NY10 | Trypanosomatidae | 27% | 100% |
A0A3Q8IBH3 | Leishmania donovani | 36% | 100% |
A4H335 | Leishmania braziliensis | 85% | 100% |
A4HRC3 | Leishmania infantum | 100% | 100% |
A4HYN5 | Leishmania infantum | 37% | 100% |
E9ABZ0 | Leishmania major | 95% | 100% |
E9AI94 | Leishmania braziliensis | 35% | 100% |
E9AJ87 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AUH9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q4QD05 | Leishmania major | 36% | 100% |
V5DS51 | Trypanosoma cruzi | 29% | 94% |