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: Q4QEM0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.458 |
CLV_PCSK_PC7_1 | 102 | 108 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.440 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.439 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.775 |
DOC_MAPK_gen_1 | 238 | 247 | PF00069 | 0.652 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.679 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.442 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.539 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.755 |
LIG_14-3-3_CanoR_1 | 106 | 110 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 164 | 173 | PF00244 | 0.813 |
LIG_14-3-3_CanoR_1 | 270 | 274 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 57 | 61 | PF00244 | 0.527 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.709 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.702 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.638 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.442 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.802 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.619 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.587 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.676 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.528 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.330 |
LIG_LIR_Gen_1 | 14 | 24 | PF02991 | 0.735 |
LIG_LIR_Gen_1 | 272 | 282 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.731 |
LIG_PTAP_UEV_1 | 134 | 139 | PF05743 | 0.542 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.485 |
LIG_SH2_NCK_1 | 112 | 116 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.485 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.702 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.643 |
MOD_CDK_SPxK_1 | 191 | 197 | PF00069 | 0.602 |
MOD_CDK_SPxxK_3 | 191 | 198 | PF00069 | 0.604 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.672 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.717 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.737 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.594 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.750 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.641 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.593 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.587 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.633 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.327 |
MOD_Cter_Amidation | 100 | 103 | PF01082 | 0.604 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.672 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.703 |
MOD_GlcNHglycan | 168 | 172 | PF01048 | 0.825 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.715 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.680 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.717 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.649 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.707 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.663 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.523 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.424 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.764 |
MOD_N-GLC_2 | 242 | 244 | PF02516 | 0.536 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.589 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.711 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.532 |
MOD_NEK2_2 | 52 | 57 | PF00069 | 0.462 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.727 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.802 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.528 |
MOD_PK_1 | 198 | 204 | PF00069 | 0.614 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.759 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.581 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.759 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.553 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.552 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.504 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.434 |
MOD_Plk_2-3 | 82 | 88 | PF00069 | 0.658 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.672 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.623 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.658 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.645 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.724 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.602 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.756 |
MOD_SUMO_for_1 | 159 | 162 | PF00179 | 0.736 |
TRG_DiLeu_BaEn_2 | 81 | 87 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 157 | 162 | PF00026 | 0.739 |
TRG_Pf-PMV_PEXEL_1 | 58 | 62 | PF00026 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HT54 | Leptomonas seymouri | 33% | 94% |
A0A3S5H6Z1 | Leishmania donovani | 87% | 100% |
A4HX42 | Leishmania infantum | 87% | 100% |
E9AQV8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |