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: E9AXY9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.818 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.659 |
CLV_PCSK_FUR_1 | 78 | 82 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.818 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.812 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.693 |
DEG_APCC_DBOX_1 | 21 | 29 | PF00400 | 0.588 |
DEG_COP1_1 | 250 | 260 | PF00400 | 0.746 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.540 |
DOC_MAPK_gen_1 | 78 | 86 | PF00069 | 0.453 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.818 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.722 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.828 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.441 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.698 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.713 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.628 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.393 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.574 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.643 |
LIG_Integrin_RGD_1 | 243 | 245 | PF01839 | 0.725 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.710 |
LIG_Pex14_1 | 210 | 214 | PF04695 | 0.686 |
LIG_Pex14_2 | 214 | 218 | PF04695 | 0.510 |
LIG_PTAP_UEV_1 | 264 | 269 | PF05743 | 0.507 |
LIG_RPA_C_Fungi | 57 | 69 | PF08784 | 0.500 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.474 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.655 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.553 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.696 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.763 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.651 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.511 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.765 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.783 |
LIG_TYR_ITIM | 197 | 202 | PF00017 | 0.551 |
LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.641 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.731 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.369 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.706 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.704 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.756 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.577 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.579 |
MOD_GlcNHglycan | 158 | 162 | PF01048 | 0.705 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.562 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.805 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.626 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.725 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.537 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.793 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.631 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.678 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.545 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.746 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.791 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.499 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.610 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.759 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.521 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.514 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.607 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.373 |
MOD_PKB_1 | 130 | 138 | PF00069 | 0.490 |
MOD_PKB_1 | 68 | 76 | PF00069 | 0.511 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.746 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.647 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.402 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.586 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.589 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.672 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.776 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.486 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.474 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.678 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.644 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.756 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.828 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.624 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.668 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.660 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.813 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M0 | Leptomonas seymouri | 41% | 87% |
A0A3Q8IDN0 | Leishmania donovani | 84% | 100% |
A4HEL4 | Leishmania braziliensis | 62% | 100% |
A4I1U5 | Leishmania infantum | 84% | 100% |
Q4Q9I5 | Leishmania major | 82% | 100% |