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 |
Related structures:
AlphaFold database: Q4QF13
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.713 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.658 |
CLV_PCSK_PC7_1 | 85 | 91 | PF00082 | 0.767 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.752 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.766 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.619 |
DOC_MAPK_gen_1 | 261 | 270 | PF00069 | 0.619 |
DOC_MAPK_gen_1 | 75 | 81 | PF00069 | 0.796 |
DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 46 | 54 | PF00069 | 0.620 |
DOC_MAPK_NFAT4_5 | 263 | 271 | PF00069 | 0.468 |
DOC_PP1_RVXF_1 | 110 | 117 | PF00149 | 0.597 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.729 |
DOC_PP2B_LxvP_1 | 268 | 271 | PF13499 | 0.480 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 372 | 376 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 75 | 80 | PF00244 | 0.817 |
LIG_AP2alpha_2 | 117 | 119 | PF02296 | 0.667 |
LIG_APCC_ABBA_1 | 116 | 121 | PF00400 | 0.678 |
LIG_CaM_NSCaTE_8 | 305 | 312 | PF13499 | 0.722 |
LIG_CtBP_PxDLS_1 | 137 | 141 | PF00389 | 0.770 |
LIG_eIF4E_1 | 273 | 279 | PF01652 | 0.643 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.721 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.549 |
LIG_GBD_Chelix_1 | 238 | 246 | PF00786 | 0.639 |
LIG_LIR_Apic_2 | 149 | 155 | PF02991 | 0.732 |
LIG_LIR_Gen_1 | 156 | 165 | PF02991 | 0.723 |
LIG_LIR_Gen_1 | 240 | 250 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.775 |
LIG_LYPXL_SIV_4 | 326 | 334 | PF13949 | 0.520 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.673 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.545 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.669 |
LIG_SH2_NCK_1 | 327 | 331 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.545 |
LIG_SH2_PTP2 | 152 | 155 | PF00017 | 0.676 |
LIG_SH2_PTP2 | 157 | 160 | PF00017 | 0.591 |
LIG_SH2_SRC | 56 | 59 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.632 |
LIG_SH2_STAT3 | 273 | 276 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.662 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.721 |
LIG_SUMO_SIM_anti_2 | 78 | 83 | PF11976 | 0.663 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.771 |
LIG_SUMO_SIM_par_1 | 348 | 354 | PF11976 | 0.669 |
LIG_TRAF2_1 | 91 | 94 | PF00917 | 0.649 |
MOD_CDC14_SPxK_1 | 73 | 76 | PF00782 | 0.738 |
MOD_CDK_SPK_2 | 101 | 106 | PF00069 | 0.711 |
MOD_CDK_SPK_2 | 70 | 75 | PF00069 | 0.676 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.733 |
MOD_CDK_SPxxK_3 | 101 | 108 | PF00069 | 0.713 |
MOD_CDK_SPxxK_3 | 70 | 77 | PF00069 | 0.735 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.716 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.595 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.618 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.604 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.735 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.793 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.656 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.535 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.672 |
MOD_Cter_Amidation | 87 | 90 | PF01082 | 0.675 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.600 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.595 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.557 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.532 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.563 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.660 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.613 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.722 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.708 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.619 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.499 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.594 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.536 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.552 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.523 |
MOD_PK_1 | 199 | 205 | PF00069 | 0.704 |
MOD_PK_1 | 75 | 81 | PF00069 | 0.816 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.804 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.697 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.733 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.786 |
MOD_PKB_1 | 293 | 301 | PF00069 | 0.653 |
MOD_PKB_1 | 75 | 83 | PF00069 | 0.815 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.680 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.390 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.669 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.598 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.734 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.763 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.747 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.494 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.693 |
MOD_SUMO_rev_2 | 139 | 146 | PF00179 | 0.678 |
TRG_DiLeu_BaEn_1 | 28 | 33 | PF01217 | 0.631 |
TRG_DiLeu_BaEn_2 | 92 | 98 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.591 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.780 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.715 |
TRG_Pf-PMV_PEXEL_1 | 112 | 117 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 225 | 230 | PF00026 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 295 | 299 | PF00026 | 0.722 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.682 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDJ0 | Leishmania donovani | 90% | 100% |
A4H8D4 | Leishmania braziliensis | 66% | 100% |
A4HWQ6 | Leishmania infantum | 90% | 100% |
E9AQG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q8IS09 | Leptomonas seymouri | 29% | 100% |