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: E9AQ85
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.630 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.554 |
CLV_Separin_Metazoa | 51 | 55 | PF03568 | 0.436 |
DEG_APCC_DBOX_1 | 98 | 106 | PF00400 | 0.426 |
DEG_SPOP_SBC_1 | 214 | 218 | PF00917 | 0.688 |
DEG_SPOP_SBC_1 | 60 | 64 | PF00917 | 0.561 |
DOC_CYCLIN_RxL_1 | 88 | 100 | PF00134 | 0.394 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.518 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 225 | 229 | PF12436 | 0.636 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.634 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.571 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 40 | 47 | PF00244 | 0.401 |
LIG_Actin_RPEL_3 | 34 | 53 | PF02755 | 0.401 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.632 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.516 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.424 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.555 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.638 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.450 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 292 | 303 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.530 |
LIG_NRP_CendR_1 | 313 | 316 | PF00754 | 0.630 |
LIG_SH2_PTP2 | 27 | 30 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.514 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.729 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.678 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.676 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.680 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.664 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.656 |
LIG_SUMO_SIM_anti_2 | 206 | 213 | PF11976 | 0.501 |
LIG_SUMO_SIM_anti_2 | 307 | 313 | PF11976 | 0.534 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.597 |
LIG_TRAF2_1 | 22 | 25 | PF00917 | 0.533 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.710 |
LIG_UBA3_1 | 95 | 103 | PF00899 | 0.419 |
LIG_WW_2 | 271 | 274 | PF00397 | 0.655 |
LIG_WW_3 | 238 | 242 | PF00397 | 0.654 |
MOD_CDK_SPxxK_3 | 87 | 94 | PF00069 | 0.415 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.636 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.709 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.693 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.734 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.614 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.635 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.696 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.539 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.486 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.693 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.506 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.562 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.708 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.487 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.705 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.606 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.594 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.674 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.657 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.714 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.623 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.630 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.645 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.575 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.764 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.431 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.488 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.561 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.618 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.761 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.622 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.682 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.573 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.567 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.535 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.711 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.530 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.576 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.519 |
MOD_PKA_1 | 40 | 46 | PF00069 | 0.432 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.716 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.349 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.412 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.465 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.650 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.573 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.711 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.549 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.650 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.544 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.677 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.758 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.712 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 91 | 96 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.514 |
TRG_NLS_MonoExtN_4 | 243 | 250 | PF00514 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WTH2 | Leishmania donovani | 75% | 98% |
A4H858 | Leishmania braziliensis | 57% | 100% |
A4HWI4 | Leishmania infantum | 74% | 98% |
Q4QF98 | Leishmania major | 74% | 98% |