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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QBV8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.672 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 98 | 106 | PF00400 | 0.522 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.654 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.409 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.715 |
DOC_CYCLIN_RxL_1 | 37 | 45 | PF00134 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 22 | 28 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 89 | 95 | PF00134 | 0.525 |
DOC_MAPK_gen_1 | 99 | 107 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 186 | 192 | PF00149 | 0.539 |
DOC_PP1_RVXF_1 | 225 | 231 | PF00149 | 0.522 |
DOC_PP2B_LxvP_1 | 89 | 92 | PF13499 | 0.579 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.672 |
DOC_USP7_MATH_2 | 139 | 145 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.583 |
LIG_BIR_III_4 | 29 | 33 | PF00653 | 0.394 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.790 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.682 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.416 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.577 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.417 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.675 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.698 |
LIG_LIR_Apic_2 | 103 | 109 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 265 | 271 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 5 | 14 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.354 |
LIG_NRBOX | 244 | 250 | PF00104 | 0.509 |
LIG_NRBOX | 7 | 13 | PF00104 | 0.575 |
LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.483 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.718 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.532 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 5 | 12 | PF11976 | 0.345 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.440 |
LIG_WRC_WIRS_1 | 200 | 205 | PF05994 | 0.434 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.747 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.607 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.607 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.427 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.622 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.480 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.496 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.517 |
MOD_Cter_Amidation | 168 | 171 | PF01082 | 0.589 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.727 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.688 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.724 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.590 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.608 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.399 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.500 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.475 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.536 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.669 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.606 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.542 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.734 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.586 |
MOD_PKB_1 | 151 | 159 | PF00069 | 0.733 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.747 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.525 |
MOD_Plk_2-3 | 3 | 9 | PF00069 | 0.546 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.733 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.570 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.617 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.745 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.646 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB35 | Leptomonas seymouri | 41% | 99% |
A0A3S7WWY3 | Leishmania donovani | 87% | 100% |
A4HC86 | Leishmania braziliensis | 61% | 92% |
A4HZR5 | Leishmania infantum | 87% | 100% |
E9AVM1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |