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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HZ86
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005515 | protein binding | 2 | 7 |
GO:0051087 | protein-folding chaperone binding | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 216 | 220 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.337 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.371 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.444 |
DOC_ANK_TNKS_1 | 132 | 139 | PF00023 | 0.613 |
DOC_MAPK_DCC_7 | 286 | 296 | PF00069 | 0.599 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.598 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.447 |
DOC_USP7_UBL2_3 | 270 | 274 | PF12436 | 0.592 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.550 |
LIG_14-3-3_CanoR_1 | 97 | 106 | PF00244 | 0.720 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.551 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.549 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.563 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.329 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.660 |
LIG_LIR_Apic_2 | 141 | 147 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 150 | 159 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.469 |
LIG_MLH1_MIPbox_1 | 149 | 153 | PF16413 | 0.551 |
LIG_Rb_LxCxE_1 | 118 | 137 | PF01857 | 0.611 |
LIG_SH2_NCK_1 | 20 | 24 | PF00017 | 0.473 |
LIG_SH2_NCK_1 | 65 | 69 | PF00017 | 0.328 |
LIG_SH2_SRC | 63 | 66 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 59 | 62 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.466 |
LIG_SH3_1 | 286 | 292 | PF00018 | 0.601 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.632 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.465 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.461 |
LIG_UBA3_1 | 44 | 51 | PF00899 | 0.454 |
MOD_CDK_SPxxK_3 | 36 | 43 | PF00069 | 0.474 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.663 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.452 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.497 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.469 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.487 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.533 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.494 |
MOD_GlcNHglycan | 14 | 18 | PF01048 | 0.678 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.337 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.481 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.427 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.684 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.704 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.751 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.376 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.488 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.481 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.638 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.564 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.499 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.745 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.563 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.420 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.436 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.492 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.498 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.571 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.362 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.386 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.502 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.486 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.651 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.591 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.558 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.647 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.376 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.508 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.584 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 163 | 168 | PF01217 | 0.566 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.431 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.596 |
TRG_NES_CRM1_1 | 253 | 267 | PF08389 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P829 | Leptomonas seymouri | 39% | 100% |
A0A1X0NYB3 | Trypanosomatidae | 31% | 75% |
A0A3Q8IB47 | Leishmania donovani | 99% | 100% |
A4HBT9 | Leishmania braziliensis | 70% | 100% |
E9AV61 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |
Q4QCC0 | Leishmania major | 89% | 100% |