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: A4H726
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.562 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.601 |
CLV_PCSK_PC1ET2_1 | 232 | 234 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.431 |
CLV_PCSK_PC7_1 | 114 | 120 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.656 |
DEG_Kelch_Keap1_1 | 279 | 284 | PF01344 | 0.611 |
DEG_ODPH_VHL_1 | 155 | 167 | PF01847 | 0.526 |
DEG_ODPH_VHL_1 | 5 | 18 | PF01847 | 0.463 |
DEG_SPOP_SBC_1 | 261 | 265 | PF00917 | 0.554 |
DOC_ANK_TNKS_1 | 117 | 124 | PF00023 | 0.521 |
DOC_CKS1_1 | 113 | 118 | PF01111 | 0.518 |
DOC_CKS1_1 | 193 | 198 | PF01111 | 0.686 |
DOC_MAPK_FxFP_2 | 29 | 32 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 118 | 126 | PF00069 | 0.523 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.578 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.534 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.520 |
LIG_14-3-3_CanoR_1 | 118 | 126 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 84 | 90 | PF00244 | 0.685 |
LIG_APCC_ABBA_1 | 341 | 346 | PF00400 | 0.518 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.463 |
LIG_EVH1_1 | 192 | 196 | PF00568 | 0.687 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.592 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.534 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.599 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.471 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.560 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.565 |
LIG_LIR_Apic_2 | 26 | 32 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 270 | 278 | PF02991 | 0.685 |
LIG_LIR_Gen_1 | 72 | 79 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 241 | 245 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.694 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.636 |
LIG_Pex14_2 | 206 | 210 | PF04695 | 0.459 |
LIG_Pex14_2 | 29 | 33 | PF04695 | 0.467 |
LIG_PTB_Apo_2 | 204 | 211 | PF02174 | 0.517 |
LIG_PTB_Apo_2 | 236 | 243 | PF02174 | 0.565 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.538 |
LIG_SH2_GRB2like | 271 | 274 | PF00017 | 0.690 |
LIG_SH2_NCK_1 | 180 | 184 | PF00017 | 0.619 |
LIG_SH2_NCK_1 | 271 | 275 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.478 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.664 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.682 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.578 |
LIG_WRC_WIRS_1 | 74 | 79 | PF05994 | 0.523 |
MOD_CDK_SPxK_1 | 112 | 118 | PF00069 | 0.519 |
MOD_CDK_SPxxK_3 | 112 | 119 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 192 | 199 | PF00069 | 0.527 |
MOD_CDK_SPxxK_3 | 75 | 82 | PF00069 | 0.529 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.584 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.667 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.497 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.530 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.524 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.554 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.687 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.614 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.557 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.726 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.759 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.548 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.698 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.482 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.489 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.549 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.651 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.539 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.667 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.687 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.692 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.510 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.528 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.522 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.572 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.714 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.692 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.600 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.578 |
MOD_OFUCOSY | 214 | 220 | PF10250 | 0.570 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.568 |
MOD_PKA_1 | 246 | 252 | PF00069 | 0.746 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.566 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.733 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.478 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.566 |
MOD_PKB_1 | 82 | 90 | PF00069 | 0.560 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.476 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.607 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.494 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.466 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.686 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.622 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.532 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.526 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.520 |
MOD_SUMO_rev_2 | 170 | 179 | PF00179 | 0.598 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.790 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.650 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.549 |
TRG_NLS_Bipartite_1 | 232 | 250 | PF00514 | 0.471 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I9J1 | Leishmania donovani | 78% | 100% |
A4HVF5 | Leishmania infantum | 75% | 100% |
E9AP53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QGD5 | Leishmania major | 79% | 100% |