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: A4HGL4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.619 |
CLV_PCSK_PC7_1 | 179 | 185 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.697 |
DEG_APCC_DBOX_1 | 275 | 283 | PF00400 | 0.737 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.775 |
DOC_MAPK_gen_1 | 183 | 192 | PF00069 | 0.688 |
DOC_MAPK_MEF2A_6 | 183 | 190 | PF00069 | 0.642 |
DOC_MAPK_NFAT4_5 | 183 | 191 | PF00069 | 0.647 |
DOC_PP1_RVXF_1 | 126 | 133 | PF00149 | 0.673 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.516 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.820 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.456 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.708 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.817 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 151 | 159 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 276 | 284 | PF00244 | 0.776 |
LIG_BRCT_BRCA1_1 | 293 | 297 | PF00533 | 0.556 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.609 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.592 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.819 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.581 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.575 |
LIG_IBAR_NPY_1 | 214 | 216 | PF08397 | 0.584 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.616 |
LIG_PCNA_TLS_4 | 88 | 95 | PF02747 | 0.522 |
LIG_RPA_C_Fungi | 174 | 186 | PF08784 | 0.653 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.623 |
LIG_SH2_CRK | 35 | 39 | PF00017 | 0.774 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.567 |
LIG_SH2_CRK | 68 | 72 | PF00017 | 0.798 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.623 |
LIG_SH2_SRC | 314 | 317 | PF00017 | 0.561 |
LIG_SH2_SRC | 68 | 71 | PF00017 | 0.757 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.735 |
LIG_SH3_1 | 67 | 73 | PF00018 | 0.546 |
LIG_SH3_2 | 108 | 113 | PF14604 | 0.567 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.539 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.571 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.468 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.833 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.711 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.546 |
LIG_SUMO_SIM_anti_2 | 157 | 163 | PF11976 | 0.603 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.823 |
LIG_WRC_WIRS_1 | 91 | 96 | PF05994 | 0.519 |
LIG_WW_3 | 13 | 17 | PF00397 | 0.549 |
MOD_CDC14_SPxK_1 | 13 | 16 | PF00782 | 0.546 |
MOD_CDC14_SPxK_1 | 218 | 221 | PF00782 | 0.625 |
MOD_CDK_SPxK_1 | 10 | 16 | PF00069 | 0.546 |
MOD_CDK_SPxK_1 | 215 | 221 | PF00069 | 0.624 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.660 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.674 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.649 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.564 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.544 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.586 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.556 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.613 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.493 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.718 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.817 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.719 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.655 |
MOD_GlcNHglycan | 172 | 176 | PF01048 | 0.557 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.823 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.715 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.530 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.699 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.803 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.589 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.664 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.636 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.592 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.660 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.673 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.749 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.646 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.800 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.646 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.719 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.725 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.560 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.772 |
MOD_N-GLC_1 | 282 | 287 | PF02516 | 0.726 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.564 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.648 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.715 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.739 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.785 |
MOD_NEK2_2 | 202 | 207 | PF00069 | 0.580 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.556 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.670 |
MOD_PK_1 | 113 | 119 | PF00069 | 0.801 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.586 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.654 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.601 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.733 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.684 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.697 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.581 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.733 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.519 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.799 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.658 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.661 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.637 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.689 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.747 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.644 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.560 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.817 |
TRG_DiLeu_BaEn_1 | 157 | 162 | PF01217 | 0.637 |
TRG_DiLeu_BaLyEn_6 | 125 | 130 | PF01217 | 0.587 |
TRG_DiLeu_LyEn_5 | 44 | 49 | PF01217 | 0.735 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.613 |
TRG_ER_diArg_1 | 79 | 82 | PF00400 | 0.642 |
TRG_NES_CRM1_1 | 157 | 170 | PF08389 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.678 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ID56 | Leishmania donovani | 74% | 99% |
A4I3P0 | Leishmania infantum | 74% | 99% |
E9AZY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 99% |
Q4Q8A4 | Leishmania major | 73% | 100% |