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: Q4QGF0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.401 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.469 |
CLV_Separin_Metazoa | 56 | 60 | PF03568 | 0.398 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.454 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.556 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.563 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.596 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 113 | 121 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 124 | 132 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 136 | 142 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 202 | 210 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 217 | 221 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 273 | 280 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.597 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.490 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.453 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.509 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.558 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.413 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.566 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.697 |
LIG_LIR_Apic_2 | 204 | 210 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.533 |
LIG_Pex14_2 | 14 | 18 | PF04695 | 0.509 |
LIG_PTAP_UEV_1 | 279 | 284 | PF05743 | 0.497 |
LIG_SH2_GRB2like | 151 | 154 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.490 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.522 |
MOD_CDK_SPxxK_3 | 43 | 50 | PF00069 | 0.533 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.692 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.569 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.555 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.623 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.555 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.543 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.486 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.459 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.684 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.535 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.604 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.511 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.434 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.644 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.441 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.537 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.619 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.438 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.572 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.564 |
MOD_PKB_1 | 103 | 111 | PF00069 | 0.400 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.538 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.510 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.438 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.532 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.555 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.552 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.628 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.622 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.606 |
MOD_SUMO_rev_2 | 86 | 92 | PF00179 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 97 | 102 | PF01217 | 0.522 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2V4 | Leptomonas seymouri | 58% | 92% |
A0A3Q8IBM3 | Leishmania donovani | 91% | 100% |
A4H712 | Leishmania braziliensis | 69% | 82% |
A4HVE0 | Leishmania infantum | 92% | 100% |
E9AP38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |