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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HKP8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.532 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.384 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.402 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.479 |
DOC_MAPK_gen_1 | 277 | 287 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 280 | 289 | PF00069 | 0.420 |
DOC_PP1_RVXF_1 | 147 | 153 | PF00149 | 0.324 |
DOC_PP1_RVXF_1 | 88 | 95 | PF00149 | 0.451 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.423 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 131 | 137 | PF00244 | 0.381 |
LIG_BIR_III_2 | 258 | 262 | PF00653 | 0.524 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.390 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.277 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.452 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.486 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.393 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.334 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.446 |
LIG_GBD_Chelix_1 | 285 | 293 | PF00786 | 0.387 |
LIG_LIR_Apic_2 | 211 | 217 | PF02991 | 0.347 |
LIG_LIR_Apic_2 | 224 | 230 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 238 | 246 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.444 |
LIG_PTAP_UEV_1 | 111 | 116 | PF05743 | 0.439 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.519 |
LIG_SH2_NCK_1 | 227 | 231 | PF00017 | 0.414 |
LIG_SH2_SRC | 11 | 14 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.461 |
LIG_SH2_STAT3 | 41 | 44 | PF00017 | 0.438 |
LIG_SH2_STAT3 | 73 | 76 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.344 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.433 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.703 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.415 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.473 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.294 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.378 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.322 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.352 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.315 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.333 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.521 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.416 |
MOD_Cter_Amidation | 349 | 352 | PF01082 | 0.541 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.479 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.440 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.315 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.498 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.485 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.728 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.777 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.342 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.301 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.350 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.614 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.611 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.383 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.332 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.248 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.473 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.381 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.299 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.332 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.350 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.409 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.430 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.515 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.474 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.454 |
MOD_PKA_1 | 351 | 357 | PF00069 | 0.535 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.484 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.614 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.701 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.321 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.329 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.384 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.419 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.272 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.285 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.714 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.364 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.346 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.454 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.351 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8A3 | Leptomonas seymouri | 74% | 100% |
A0A0S4J2R9 | Bodo saltans | 43% | 96% |
A0A1X0NRV1 | Trypanosomatidae | 43% | 100% |
A0A3Q8IDA1 | Leishmania donovani | 84% | 83% |
A0A3R7L0G4 | Trypanosoma rangeli | 52% | 100% |
A4I879 | Leishmania infantum | 84% | 83% |
D0AAE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9B337 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q517 | Leishmania major | 86% | 100% |
V5BET5 | Trypanosoma cruzi | 52% | 88% |