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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A0A3S7X9U4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.455 |
CLV_PCSK_FUR_1 | 57 | 61 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 129 | 131 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 284 | 286 | PF00082 | 0.441 |
CLV_PCSK_PC7_1 | 68 | 74 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.465 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.572 |
DEG_SCF_FBW7_1 | 8 | 13 | PF00400 | 0.408 |
DEG_SPOP_SBC_1 | 95 | 99 | PF00917 | 0.775 |
DOC_CYCLIN_RxL_1 | 282 | 292 | PF00134 | 0.728 |
DOC_CYCLIN_yClb1_LxF_4 | 221 | 226 | PF00134 | 0.741 |
DOC_CYCLIN_yCln2_LP_2 | 139 | 145 | PF00134 | 0.764 |
DOC_MAPK_gen_1 | 129 | 137 | PF00069 | 0.666 |
DOC_MAPK_JIP1_4 | 185 | 191 | PF00069 | 0.672 |
DOC_MAPK_MEF2A_6 | 185 | 193 | PF00069 | 0.821 |
DOC_PP1_RVXF_1 | 221 | 227 | PF00149 | 0.743 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.733 |
DOC_PP2B_LxvP_1 | 189 | 192 | PF13499 | 0.771 |
DOC_PP4_FxxP_1 | 226 | 229 | PF00568 | 0.751 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.690 |
DOC_USP7_MATH_2 | 103 | 109 | PF00917 | 0.761 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.641 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 185 | 190 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 260 | 268 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 77 | 86 | PF00244 | 0.651 |
LIG_CSL_BTD_1 | 135 | 138 | PF09270 | 0.744 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.694 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.850 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.673 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.746 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.807 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.646 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.432 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.800 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.585 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.716 |
LIG_LIR_Gen_1 | 13 | 20 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.482 |
LIG_MYND_1 | 138 | 142 | PF01753 | 0.747 |
LIG_NRBOX | 23 | 29 | PF00104 | 0.415 |
LIG_PALB2_WD40_1 | 132 | 140 | PF16756 | 0.740 |
LIG_PCNA_yPIPBox_3 | 267 | 281 | PF02747 | 0.719 |
LIG_Rb_LxCxE_1 | 49 | 63 | PF01857 | 0.653 |
LIG_SH2_GRB2like | 20 | 23 | PF00017 | 0.398 |
LIG_SH2_GRB2like | 244 | 247 | PF00017 | 0.705 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.711 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.720 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.665 |
LIG_SUMO_SIM_anti_2 | 25 | 31 | PF11976 | 0.419 |
LIG_TYR_ITIM | 29 | 34 | PF00017 | 0.513 |
MOD_CDC14_SPxK_1 | 152 | 155 | PF00782 | 0.711 |
MOD_CDK_SPxK_1 | 149 | 155 | PF00069 | 0.713 |
MOD_CDK_SPxK_1 | 6 | 12 | PF00069 | 0.547 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.676 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.705 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.711 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.712 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.660 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.491 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.559 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.722 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.742 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.570 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.763 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.687 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.527 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.458 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.626 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.710 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.757 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.706 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.609 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.713 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.706 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.704 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.725 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.751 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.499 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.654 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.776 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.689 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.644 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.746 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.736 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.775 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.737 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.677 |
MOD_N-GLC_2 | 148 | 150 | PF02516 | 0.575 |
MOD_N-GLC_2 | 256 | 258 | PF02516 | 0.644 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.679 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.668 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.533 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.645 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.674 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.476 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.572 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.712 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.630 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.763 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.492 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.692 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.716 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.666 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.547 |
MOD_SUMO_rev_2 | 125 | 135 | PF00179 | 0.586 |
TRG_DiLeu_BaEn_1 | 25 | 30 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.694 |
TRG_DiLeu_BaLyEn_6 | 216 | 221 | PF01217 | 0.566 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.656 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 12 | 16 | PF00026 | 0.626 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK89 | Leptomonas seymouri | 34% | 100% |
A4HN98 | Leishmania braziliensis | 63% | 100% |
A4IBW9 | Leishmania infantum | 100% | 100% |
E9AFQ6 | Leishmania major | 85% | 100% |
E9B6V9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |