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: E9B6D9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.765 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.640 |
CLV_PCSK_FUR_1 | 33 | 37 | PF00082 | 0.602 |
CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.818 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.640 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 269 | 271 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.627 |
DEG_APCC_DBOX_1 | 269 | 277 | PF00400 | 0.485 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.697 |
DOC_CDC14_PxL_1 | 288 | 296 | PF14671 | 0.468 |
DOC_CKS1_1 | 224 | 229 | PF01111 | 0.647 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.675 |
DOC_CKS1_1 | 91 | 96 | PF01111 | 0.608 |
DOC_MAPK_gen_1 | 193 | 199 | PF00069 | 0.519 |
DOC_MAPK_gen_1 | 269 | 275 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 269 | 277 | PF00069 | 0.485 |
DOC_PP4_FxxP_1 | 322 | 325 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.666 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.723 |
DOC_USP7_UBL2_3 | 182 | 186 | PF12436 | 0.575 |
DOC_USP7_UBL2_3 | 35 | 39 | PF12436 | 0.668 |
DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.683 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.751 |
LIG_14-3-3_CanoR_1 | 108 | 114 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 256 | 266 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 312 | 320 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.583 |
LIG_EVH1_1 | 188 | 192 | PF00568 | 0.503 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.688 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.653 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.507 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.550 |
LIG_Integrin_isoDGR_2 | 297 | 299 | PF01839 | 0.554 |
LIG_LIR_Apic_2 | 317 | 323 | PF02991 | 0.478 |
LIG_RPA_C_Fungi | 204 | 216 | PF08784 | 0.580 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.497 |
LIG_SH3_1 | 103 | 109 | PF00018 | 0.561 |
LIG_SH3_1 | 186 | 192 | PF00018 | 0.558 |
LIG_SH3_1 | 215 | 221 | PF00018 | 0.619 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.638 |
LIG_SH3_1 | 88 | 94 | PF00018 | 0.617 |
LIG_SH3_2 | 106 | 111 | PF14604 | 0.594 |
LIG_SH3_2 | 189 | 194 | PF14604 | 0.674 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.716 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.579 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.525 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.705 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.776 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.465 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.449 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.692 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.699 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.654 |
LIG_SH3_5 | 10 | 14 | PF00018 | 0.510 |
LIG_UBA3_1 | 264 | 269 | PF00899 | 0.279 |
MOD_CDK_SPxK_1 | 132 | 138 | PF00069 | 0.665 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.675 |
MOD_CDK_SPxxK_3 | 153 | 160 | PF00069 | 0.528 |
MOD_CDK_SPxxK_3 | 90 | 97 | PF00069 | 0.585 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.448 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.445 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.639 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.548 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.651 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.417 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.587 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.461 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.486 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.450 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.652 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.585 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.503 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.506 |
MOD_NEK2_2 | 315 | 320 | PF00069 | 0.441 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.606 |
MOD_PKA_1 | 35 | 41 | PF00069 | 0.666 |
MOD_PKA_1 | 61 | 67 | PF00069 | 0.666 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.715 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.693 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.452 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.669 |
MOD_PKB_1 | 146 | 154 | PF00069 | 0.568 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.575 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.435 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.686 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.312 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.543 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.483 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.628 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.665 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.529 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.647 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.715 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.704 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.752 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.598 |
TRG_NLS_MonoExtC_3 | 268 | 274 | PF00514 | 0.463 |
TRG_NLS_MonoExtC_3 | 34 | 39 | PF00514 | 0.615 |
TRG_NLS_MonoExtN_4 | 33 | 39 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 299 | 304 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IF70 | Leishmania donovani | 87% | 100% |
A4HMT0 | Leishmania braziliensis | 61% | 90% |
A4IBC8 | Leishmania infantum | 87% | 100% |
E9AF84 | Leishmania major | 86% | 100% |