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: A4HEL4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.650 |
CLV_PCSK_FUR_1 | 78 | 82 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.793 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.398 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.697 |
DOC_CYCLIN_yCln2_LP_2 | 210 | 216 | PF00134 | 0.494 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 78 | 86 | PF00069 | 0.467 |
DOC_PP1_RVXF_1 | 25 | 31 | PF00149 | 0.393 |
DOC_PP1_RVXF_1 | 80 | 87 | PF00149 | 0.431 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.441 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.815 |
LIG_14-3-3_CanoR_1 | 113 | 117 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 138 | 147 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 81 | 87 | PF00244 | 0.663 |
LIG_BIR_III_2 | 296 | 300 | PF00653 | 0.570 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.471 |
LIG_Integrin_RGD_1 | 243 | 245 | PF01839 | 0.690 |
LIG_LIR_Gen_1 | 150 | 161 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 20 | 28 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 85 | 89 | PF02991 | 0.538 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.668 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.513 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.702 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.604 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.761 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.627 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.499 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.750 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.415 |
LIG_TYR_ITIM | 197 | 202 | PF00017 | 0.542 |
LIG_UBA3_1 | 24 | 33 | PF00899 | 0.397 |
LIG_WRC_WIRS_1 | 83 | 88 | PF05994 | 0.429 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.682 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.750 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.462 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.686 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.613 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.581 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.637 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.585 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.646 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.605 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.563 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.630 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.542 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.587 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.695 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.662 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.650 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.584 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.746 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.785 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.507 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.588 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.454 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.355 |
MOD_PKB_1 | 130 | 138 | PF00069 | 0.493 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.642 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.644 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.611 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.565 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.592 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.582 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.549 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.737 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.648 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.631 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.765 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.817 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.664 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.671 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.771 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.674 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M0 | Leptomonas seymouri | 39% | 87% |
A0A3Q8IDN0 | Leishmania donovani | 63% | 100% |
A4I1U5 | Leishmania infantum | 63% | 100% |
E9AXY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4Q9I5 | Leishmania major | 64% | 100% |