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: Q4Q8G1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.727 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.645 |
CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.668 |
CLV_PCSK_PC7_1 | 15 | 21 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.619 |
DEG_COP1_1 | 130 | 137 | PF00400 | 0.665 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.589 |
DOC_PP4_FxxP_1 | 258 | 261 | PF00568 | 0.690 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.690 |
DOC_USP7_UBL2_3 | 284 | 288 | PF12436 | 0.685 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.755 |
LIG_14-3-3_CanoR_1 | 123 | 127 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.631 |
LIG_APCC_ABBA_1 | 325 | 330 | PF00400 | 0.557 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.690 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.648 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.792 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.700 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.593 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.580 |
LIG_LIR_Apic_2 | 255 | 261 | PF02991 | 0.681 |
LIG_LIR_Gen_1 | 153 | 163 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.585 |
LIG_MYND_1 | 401 | 405 | PF01753 | 0.583 |
LIG_SH2_GRB2like | 302 | 305 | PF00017 | 0.721 |
LIG_SH2_SRC | 302 | 305 | PF00017 | 0.615 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.696 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.665 |
LIG_SH2_STAT3 | 316 | 319 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.653 |
LIG_SH3_1 | 201 | 207 | PF00018 | 0.624 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.530 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.642 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.589 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.706 |
LIG_SH3_4 | 284 | 291 | PF00018 | 0.688 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.748 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.514 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.742 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.570 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.819 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.691 |
MOD_Cter_Amidation | 208 | 211 | PF01082 | 0.697 |
MOD_Cter_Amidation | 22 | 25 | PF01082 | 0.613 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.738 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.691 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.775 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.733 |
MOD_GlcNHglycan | 226 | 230 | PF01048 | 0.765 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.663 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.772 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.619 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.652 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.828 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.724 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.799 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.520 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.631 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.575 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.721 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.693 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.719 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.555 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.613 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.680 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.760 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.613 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.635 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.743 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.680 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.760 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.664 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.541 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.723 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.635 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.706 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.755 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.764 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P454 | Leptomonas seymouri | 41% | 100% |
A0A3S7X1G1 | Leishmania donovani | 91% | 100% |
A4HGF0 | Leishmania braziliensis | 62% | 100% |
A4I3I1 | Leishmania infantum | 91% | 100% |
E9AZS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |