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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A4HCJ9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.701 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.589 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.589 |
CLV_PCSK_PC7_1 | 311 | 317 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.751 |
DEG_COP1_1 | 23 | 31 | PF00400 | 0.578 |
DOC_CDC14_PxL_1 | 77 | 85 | PF14671 | 0.606 |
DOC_MAPK_MEF2A_6 | 209 | 217 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 254 | 261 | PF00149 | 0.752 |
DOC_PP1_SILK_1 | 293 | 298 | PF00149 | 0.571 |
DOC_PP2B_LxvP_1 | 78 | 81 | PF13499 | 0.671 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.571 |
DOC_USP7_MATH_2 | 67 | 73 | PF00917 | 0.582 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 322 | 329 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.623 |
LIG_APCC_ABBA_1 | 205 | 210 | PF00400 | 0.537 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.612 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.655 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.585 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.750 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.598 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.617 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.706 |
LIG_LIR_Gen_1 | 226 | 235 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.736 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.745 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.605 |
LIG_MYND_1 | 106 | 110 | PF01753 | 0.576 |
LIG_PCNA_PIPBox_1 | 224 | 233 | PF02747 | 0.723 |
LIG_SH2_CRK | 267 | 271 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.599 |
LIG_SH3_1 | 148 | 154 | PF00018 | 0.594 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.569 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.675 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.799 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.732 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.555 |
LIG_SUMO_SIM_anti_2 | 99 | 105 | PF11976 | 0.560 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.590 |
LIG_WRC_WIRS_1 | 306 | 311 | PF05994 | 0.546 |
LIG_WW_3 | 73 | 77 | PF00397 | 0.585 |
MOD_CDC14_SPxK_1 | 109 | 112 | PF00782 | 0.573 |
MOD_CDC14_SPxK_1 | 169 | 172 | PF00782 | 0.737 |
MOD_CDC14_SPxK_1 | 244 | 247 | PF00782 | 0.592 |
MOD_CDK_SPxK_1 | 106 | 112 | PF00069 | 0.575 |
MOD_CDK_SPxK_1 | 166 | 172 | PF00069 | 0.738 |
MOD_CDK_SPxK_1 | 241 | 247 | PF00069 | 0.591 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.652 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.694 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.685 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.749 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.596 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.595 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.549 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.568 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.690 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.608 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.618 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.725 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.603 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.520 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.708 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.739 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.637 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.640 |
MOD_N-GLC_2 | 157 | 159 | PF02516 | 0.606 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.721 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.590 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.721 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.717 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.546 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.589 |
MOD_NEK2_2 | 305 | 310 | PF00069 | 0.533 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.616 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.706 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.580 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.689 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.746 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.544 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.739 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.511 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.715 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.560 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.674 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.762 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.714 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.579 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.680 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.647 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3L3 | Leptomonas seymouri | 36% | 100% |
A0A3S7WXD1 | Leishmania donovani | 55% | 100% |