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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HHG0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.441 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.419 |
DEG_SCF_FBW7_1 | 228 | 235 | PF00400 | 0.660 |
DOC_AGCK_PIF_1 | 37 | 42 | PF00069 | 0.571 |
DOC_ANK_TNKS_1 | 81 | 88 | PF00023 | 0.614 |
DOC_CKS1_1 | 229 | 234 | PF01111 | 0.661 |
DOC_CYCLIN_RxL_1 | 223 | 231 | PF00134 | 0.640 |
DOC_MAPK_DCC_7 | 103 | 113 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 286 | 294 | PF00069 | 0.797 |
DOC_PP4_FxxP_1 | 136 | 139 | PF00568 | 0.687 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.564 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.593 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 124 | 133 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 233 | 239 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 39 | 45 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 99 | 107 | PF00244 | 0.660 |
LIG_Actin_WH2_2 | 25 | 41 | PF00022 | 0.269 |
LIG_APCC_ABBA_1 | 114 | 119 | PF00400 | 0.586 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.633 |
LIG_EVH1_2 | 45 | 49 | PF00568 | 0.553 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.731 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.617 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.584 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.579 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.339 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.549 |
LIG_LIR_Apic_2 | 41 | 45 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 10 | 20 | PF02991 | 0.250 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.605 |
LIG_Pex14_1 | 320 | 324 | PF04695 | 0.633 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.640 |
LIG_SH2_NCK_1 | 252 | 256 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 324 | 328 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.605 |
LIG_SH3_1 | 103 | 109 | PF00018 | 0.622 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.631 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.683 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.727 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.269 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.440 |
LIG_SUMO_SIM_anti_2 | 329 | 336 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 339 | 345 | PF11976 | 0.269 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.665 |
LIG_TRFH_1 | 42 | 46 | PF08558 | 0.565 |
LIG_WW_1 | 45 | 48 | PF00397 | 0.556 |
MOD_CDK_SPK_2 | 228 | 233 | PF00069 | 0.663 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.642 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.682 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.640 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.639 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.711 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.548 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.554 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.654 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.622 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.606 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.611 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.531 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.307 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.612 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.452 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.707 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.824 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.805 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.671 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.707 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.752 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.615 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.269 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.589 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.563 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.768 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.689 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.718 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.769 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.643 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.575 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.572 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.545 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.631 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.681 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.568 |
MOD_PK_1 | 244 | 250 | PF00069 | 0.606 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.647 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.569 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.657 |
MOD_PKB_1 | 177 | 185 | PF00069 | 0.694 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.712 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.638 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.601 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.574 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.489 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.552 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.589 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.639 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.706 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.824 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.713 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.625 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.555 |
MOD_SUMO_rev_2 | 183 | 188 | PF00179 | 0.658 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.641 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.712 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7L3 | Leishmania donovani | 61% | 100% |
A4I4L0 | Leishmania infantum | 60% | 100% |
E9AE07 | Leishmania major | 53% | 100% |
E9ALS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |