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: A4HQ66
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.559 |
DEG_APCC_DBOX_1 | 272 | 280 | PF00400 | 0.554 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.736 |
DOC_CKS1_1 | 227 | 232 | PF01111 | 0.432 |
DOC_CYCLIN_RxL_1 | 272 | 282 | PF00134 | 0.551 |
DOC_PP4_FxxP_1 | 227 | 230 | PF00568 | 0.447 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.492 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 116 | 126 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 128 | 136 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 144 | 152 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 166 | 170 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 248 | 258 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 73 | 81 | PF00244 | 0.615 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.641 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.498 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.531 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.586 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.767 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.613 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.512 |
LIG_GSK3_LRP6_1 | 210 | 215 | PF00069 | 0.500 |
LIG_LIR_Apic_2 | 224 | 230 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 120 | 130 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 93 | 104 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.578 |
LIG_NRBOX | 275 | 281 | PF00104 | 0.548 |
LIG_Pex14_1 | 235 | 239 | PF04695 | 0.396 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.384 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.599 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.493 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.567 |
LIG_SUMO_SIM_par_1 | 275 | 282 | PF11976 | 0.551 |
LIG_TRAF2_2 | 86 | 91 | PF00917 | 0.547 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.622 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.516 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.682 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.589 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.522 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.735 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.420 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.441 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.598 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.580 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.650 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.694 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.511 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.596 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.684 |
MOD_GlcNHglycan | 289 | 294 | PF01048 | 0.647 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.641 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.629 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.626 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.666 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.638 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.592 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.619 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.659 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.716 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.506 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.607 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.629 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.586 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.559 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.553 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.565 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.597 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.599 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.644 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.581 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.593 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.562 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.580 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.695 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.622 |
MOD_Plk_2-3 | 36 | 42 | PF00069 | 0.421 |
MOD_Plk_2-3 | 77 | 83 | PF00069 | 0.668 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.416 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.658 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.595 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.436 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 272 | 277 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.575 |
TRG_ER_diArg_1 | 273 | 276 | PF00400 | 0.563 |
TRG_NES_CRM1_1 | 274 | 289 | PF08389 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IWF6 | Leishmania donovani | 64% | 100% |
A4IDW3 | Leishmania infantum | 63% | 100% |
E9ATY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4Q0L2 | Leishmania major | 63% | 98% |