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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AP40
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.732 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.527 |
CLV_PCSK_FUR_1 | 90 | 94 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.656 |
CLV_Separin_Metazoa | 324 | 328 | PF03568 | 0.649 |
DOC_CKS1_1 | 24 | 29 | PF01111 | 0.642 |
DOC_CYCLIN_RxL_1 | 17 | 26 | PF00134 | 0.699 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 378 | 387 | PF00134 | 0.644 |
DOC_MAPK_gen_1 | 221 | 231 | PF00069 | 0.645 |
DOC_MAPK_gen_1 | 40 | 48 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 73 | 81 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 74 | 83 | PF00069 | 0.643 |
DOC_PP1_RVXF_1 | 106 | 112 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 22 | 25 | PF13499 | 0.702 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.738 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.703 |
LIG_14-3-3_CanoR_1 | 108 | 112 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 120 | 129 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 224 | 231 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 253 | 263 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.643 |
LIG_14-3-3_CterR_2 | 390 | 393 | PF00244 | 0.456 |
LIG_Actin_WH2_2 | 311 | 329 | PF00022 | 0.646 |
LIG_APCC_ABBA_1 | 375 | 380 | PF00400 | 0.429 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.473 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.668 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.674 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.661 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.663 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.639 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.579 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.705 |
LIG_Integrin_RGD_1 | 214 | 216 | PF01839 | 0.698 |
LIG_LIR_Gen_1 | 145 | 154 | PF02991 | 0.771 |
LIG_LIR_Gen_1 | 169 | 178 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.757 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.621 |
LIG_PCNA_yPIPBox_3 | 73 | 87 | PF02747 | 0.558 |
LIG_PDZ_Class_1 | 388 | 393 | PF00595 | 0.531 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.629 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.448 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.500 |
LIG_SH2_STAT3 | 55 | 58 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.609 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.669 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.736 |
LIG_SUMO_SIM_par_1 | 360 | 367 | PF11976 | 0.636 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.443 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.646 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.664 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.481 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.499 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.717 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.717 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.679 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.726 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.560 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.705 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.615 |
MOD_DYRK1A_RPxSP_1 | 12 | 16 | PF00069 | 0.733 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.685 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.721 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.685 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.556 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.556 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.536 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.582 |
MOD_GlcNHglycan | 332 | 336 | PF01048 | 0.644 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.757 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.595 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.625 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.569 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.717 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.531 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.508 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.692 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.505 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.624 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.667 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.739 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.697 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.648 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.655 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.513 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.710 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.662 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.639 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.400 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.686 |
MOD_PK_1 | 202 | 208 | PF00069 | 0.513 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.566 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.665 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.701 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.637 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.725 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.564 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.522 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.572 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.582 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.623 |
MOD_Plk_1 | 385 | 391 | PF00069 | 0.642 |
MOD_Plk_2-3 | 144 | 150 | PF00069 | 0.695 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.457 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.722 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.555 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.669 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.681 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.657 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.618 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.699 |
MOD_SUMO_rev_2 | 348 | 354 | PF00179 | 0.751 |
TRG_DiLeu_BaEn_4 | 104 | 110 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 218 | 223 | PF01217 | 0.566 |
TRG_DiLeu_BaLyEn_6 | 342 | 347 | PF01217 | 0.694 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.560 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 326 | 328 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.535 |
TRG_PTS1 | 390 | 393 | PF00515 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1S5 | Leptomonas seymouri | 45% | 86% |
A0A1X0NNN8 | Trypanosomatidae | 25% | 72% |
A0A3R7MBM6 | Trypanosoma rangeli | 25% | 77% |
A0A3S5H6M8 | Leishmania donovani | 89% | 71% |
A4H714 | Leishmania braziliensis | 75% | 100% |
A4HVE2 | Leishmania infantum | 88% | 71% |
Q4QGE8 | Leishmania major | 87% | 100% |