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: E9AF84
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.761 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.703 |
CLV_PCSK_FUR_1 | 33 | 37 | PF00082 | 0.661 |
CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.703 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.786 |
CLV_PCSK_PC1ET2_1 | 270 | 272 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.769 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.640 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.544 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.758 |
DEG_SCF_FBW7_1 | 188 | 195 | PF00400 | 0.670 |
DOC_CDC14_PxL_1 | 289 | 297 | PF14671 | 0.507 |
DOC_CKS1_1 | 184 | 189 | PF01111 | 0.672 |
DOC_CKS1_1 | 225 | 230 | PF01111 | 0.698 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.589 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.713 |
DOC_CYCLIN_yCln2_LP_2 | 42 | 48 | PF00134 | 0.587 |
DOC_MAPK_gen_1 | 270 | 276 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 270 | 278 | PF00069 | 0.544 |
DOC_PP4_FxxP_1 | 323 | 326 | PF00568 | 0.601 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.696 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.782 |
DOC_USP7_UBL2_3 | 35 | 39 | PF12436 | 0.730 |
DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.720 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 108 | 118 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 131 | 136 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 257 | 267 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 313 | 321 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.635 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.754 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.701 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.311 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.556 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.623 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.499 |
LIG_Integrin_isoDGR_2 | 298 | 300 | PF01839 | 0.607 |
LIG_LIR_Apic_2 | 318 | 324 | PF02991 | 0.530 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.549 |
LIG_SH3_1 | 216 | 222 | PF00018 | 0.654 |
LIG_SH3_2 | 189 | 194 | PF14604 | 0.745 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.764 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.763 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.715 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.513 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.476 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.735 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.739 |
LIG_SH3_5 | 10 | 14 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 241 | 248 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 241 | 250 | PF11976 | 0.462 |
MOD_CDK_SPK_2 | 188 | 193 | PF00069 | 0.671 |
MOD_CDK_SPxK_1 | 132 | 138 | PF00069 | 0.643 |
MOD_CDK_SPxK_1 | 188 | 194 | PF00069 | 0.670 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.710 |
MOD_CDK_SPxxK_3 | 96 | 103 | PF00069 | 0.620 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.666 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.443 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.563 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.546 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.635 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.654 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.352 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.708 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.659 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.502 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.596 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.670 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.528 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.528 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.365 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.376 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.666 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.552 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.602 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.681 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.593 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.552 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.554 |
MOD_NEK2_2 | 316 | 321 | PF00069 | 0.480 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.618 |
MOD_PKA_1 | 110 | 116 | PF00069 | 0.680 |
MOD_PKA_1 | 35 | 41 | PF00069 | 0.679 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.766 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.761 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.494 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.679 |
MOD_PKB_1 | 108 | 116 | PF00069 | 0.676 |
MOD_PKB_1 | 129 | 137 | PF00069 | 0.660 |
MOD_PKB_1 | 146 | 154 | PF00069 | 0.572 |
MOD_PKB_1 | 210 | 218 | PF00069 | 0.549 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.542 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.276 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.475 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.588 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.738 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.524 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.305 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.593 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.535 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.661 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.643 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.672 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.697 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.633 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.771 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.678 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 1 | 4 | PF00179 | 0.666 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 129 | 132 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.747 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.647 |
TRG_NLS_MonoCore_2 | 102 | 107 | PF00514 | 0.602 |
TRG_NLS_MonoExtC_3 | 269 | 275 | PF00514 | 0.526 |
TRG_NLS_MonoExtC_3 | 34 | 39 | PF00514 | 0.664 |
TRG_NLS_MonoExtN_4 | 100 | 107 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 33 | 39 | PF00514 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 300 | 305 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IF70 | Leishmania donovani | 89% | 100% |
A4HMT0 | Leishmania braziliensis | 62% | 100% |
A4IBC8 | Leishmania infantum | 88% | 100% |
E9B6D9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |