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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4H6V6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.621 |
CLV_PCSK_FUR_1 | 225 | 229 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.475 |
DEG_SPOP_SBC_1 | 151 | 155 | PF00917 | 0.544 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.551 |
DOC_CYCLIN_yClb3_PxF_3 | 356 | 362 | PF00134 | 0.550 |
DOC_MAPK_gen_1 | 271 | 279 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.516 |
DOC_PP1_RVXF_1 | 161 | 167 | PF00149 | 0.516 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.557 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.633 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.553 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 198 | 208 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.478 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.504 |
LIG_BIR_III_2 | 12 | 16 | PF00653 | 0.533 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 293 | 297 | PF00533 | 0.677 |
LIG_EH_1 | 294 | 298 | PF12763 | 0.615 |
LIG_eIF4E_1 | 159 | 165 | PF01652 | 0.594 |
LIG_EVH1_2 | 360 | 364 | PF00568 | 0.552 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.545 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.692 |
LIG_IRF3_LxIS_1 | 35 | 42 | PF10401 | 0.656 |
LIG_LIR_Apic_2 | 294 | 300 | PF02991 | 0.546 |
LIG_LIR_Apic_2 | 84 | 89 | PF02991 | 0.648 |
LIG_LIR_Gen_1 | 26 | 36 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 72 | 83 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.690 |
LIG_MYND_1 | 296 | 300 | PF01753 | 0.552 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.678 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.652 |
LIG_SH2_SRC | 70 | 73 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 129 | 133 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.566 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.618 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.552 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.721 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.564 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.554 |
LIG_SUMO_SIM_par_1 | 334 | 339 | PF11976 | 0.636 |
MOD_CDC14_SPxK_1 | 179 | 182 | PF00782 | 0.721 |
MOD_CDK_SPK_2 | 114 | 119 | PF00069 | 0.555 |
MOD_CDK_SPK_2 | 64 | 69 | PF00069 | 0.593 |
MOD_CDK_SPxK_1 | 176 | 182 | PF00069 | 0.718 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.695 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.666 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.521 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.670 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.544 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.551 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.614 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.553 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.682 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.596 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.776 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.656 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.532 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.756 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.645 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.675 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.514 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.636 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.719 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.669 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.505 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.550 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.516 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.555 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.539 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.686 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.756 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.642 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.615 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.658 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.551 |
MOD_PKA_1 | 81 | 87 | PF00069 | 0.481 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.742 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.544 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.537 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.548 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.494 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.608 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.642 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.723 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.714 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.789 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.705 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.494 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.673 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.587 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.568 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.721 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.680 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.485 |
TRG_DiLeu_BaEn_2 | 161 | 167 | PF01217 | 0.516 |
TRG_DiLeu_LyEn_5 | 160 | 165 | PF01217 | 0.680 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.548 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H6K7 | Leishmania donovani | 62% | 89% |
E9AGC8 | Leishmania infantum | 62% | 89% |
E9ANW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 93% |
Q4QGQ2 | Leishmania major | 58% | 100% |