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: E9AK95
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.752 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.486 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.547 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.488 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.467 |
DEG_SPOP_SBC_1 | 288 | 292 | PF00917 | 0.476 |
DOC_CKS1_1 | 44 | 49 | PF01111 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 282 | 288 | PF00134 | 0.487 |
DOC_MAPK_gen_1 | 20 | 26 | PF00069 | 0.517 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.493 |
DOC_PP4_FxxP_1 | 78 | 81 | PF00568 | 0.490 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 91 | 95 | PF12436 | 0.602 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 138 | 147 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 20 | 24 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.564 |
LIG_AP2alpha_2 | 112 | 114 | PF02296 | 0.562 |
LIG_BRCT_BRCA1_1 | 44 | 48 | PF00533 | 0.477 |
LIG_deltaCOP1_diTrp_1 | 112 | 117 | PF00928 | 0.592 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.517 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.487 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.597 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.475 |
LIG_LIR_Gen_1 | 112 | 119 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.592 |
LIG_MYND_1 | 216 | 220 | PF01753 | 0.400 |
LIG_PTAP_UEV_1 | 3 | 8 | PF05743 | 0.462 |
LIG_SH2_NCK_1 | 302 | 306 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.736 |
LIG_SH3_1 | 309 | 315 | PF00018 | 0.636 |
LIG_SH3_2 | 4 | 9 | PF14604 | 0.469 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.506 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.566 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.513 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.524 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.804 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.689 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.599 |
LIG_SH3_4 | 91 | 98 | PF00018 | 0.576 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.578 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.618 |
LIG_WW_3 | 108 | 112 | PF00397 | 0.629 |
MOD_CDK_SPK_2 | 325 | 330 | PF00069 | 0.776 |
MOD_CDK_SPxxK_3 | 216 | 223 | PF00069 | 0.398 |
MOD_CDK_SPxxK_3 | 43 | 50 | PF00069 | 0.476 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.648 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.677 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.493 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.615 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.578 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.615 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.451 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.543 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.475 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.786 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.704 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.683 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.633 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.562 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.560 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.489 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.566 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.647 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.720 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.606 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.527 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.599 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.546 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.536 |
MOD_LATS_1 | 164 | 170 | PF00433 | 0.641 |
MOD_LATS_1 | 84 | 90 | PF00433 | 0.629 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.589 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.582 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.539 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.804 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.527 |
MOD_PK_1 | 166 | 172 | PF00069 | 0.642 |
MOD_PKA_1 | 250 | 256 | PF00069 | 0.497 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.581 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.644 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.683 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.794 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.520 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.597 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.505 |
MOD_PKB_1 | 136 | 144 | PF00069 | 0.523 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.627 |
MOD_Plk_2-3 | 118 | 124 | PF00069 | 0.574 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.521 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.397 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.792 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.717 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.729 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIT4 | Leptomonas seymouri | 36% | 100% |
A0A3S5H5F0 | Leishmania donovani | 84% | 100% |
A4H428 | Leishmania braziliensis | 56% | 100% |
A4HSB2 | Leishmania infantum | 84% | 100% |
O97195 | Leishmania major | 81% | 100% |