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 |
Related structures:
AlphaFold database: A4HG64
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.433 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.702 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.639 |
DOC_MAPK_gen_1 | 267 | 277 | PF00069 | 0.496 |
DOC_PIKK_1 | 139 | 147 | PF02985 | 0.562 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.541 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.664 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 199 | 209 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 224 | 228 | PF00244 | 0.706 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.552 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.640 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.546 |
LIG_eIF4E_1 | 81 | 87 | PF01652 | 0.521 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.622 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.693 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.805 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.551 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.703 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.721 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.661 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.637 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 11 | 19 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 92 | 102 | PF02991 | 0.759 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.758 |
LIG_NRBOX | 178 | 184 | PF00104 | 0.533 |
LIG_PCNA_PIPBox_1 | 281 | 290 | PF02747 | 0.418 |
LIG_PDZ_Class_2 | 331 | 336 | PF00595 | 0.642 |
LIG_Pex14_2 | 328 | 332 | PF04695 | 0.623 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.629 |
LIG_SH2_NCK_1 | 165 | 169 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.630 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.686 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.717 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.506 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.556 |
LIG_SUMO_SIM_par_1 | 15 | 20 | PF11976 | 0.537 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.668 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.548 |
LIG_TRAF2_1 | 276 | 279 | PF00917 | 0.608 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.585 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.537 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.650 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.531 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.720 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.698 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.582 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.535 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.735 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.537 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.594 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.590 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.698 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.644 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.603 |
MOD_GlcNHglycan | 114 | 118 | PF01048 | 0.691 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.536 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.690 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.546 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.610 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.693 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.776 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.625 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.641 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.643 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.678 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.552 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.703 |
MOD_LATS_1 | 6 | 12 | PF00433 | 0.522 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.561 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.523 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.544 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.632 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.543 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.538 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.642 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.647 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.559 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.640 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.639 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.590 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.544 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.704 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.558 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.726 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.548 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.561 |
MOD_Plk_2-3 | 212 | 218 | PF00069 | 0.551 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.715 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.606 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.520 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.651 |
MOD_SUMO_rev_2 | 190 | 198 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 233 | 243 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_4 | 139 | 145 | PF01217 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 178 | 183 | PF01217 | 0.675 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.724 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 181 | 186 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHW6 | Leishmania donovani | 55% | 100% |
A4I396 | Leishmania infantum | 55% | 100% |
E9AZI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
Q4Q8P7 | Leishmania major | 52% | 100% |