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: 1, no: 5 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3S7WVU6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 398 | 402 | PF00656 | 0.702 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.758 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.573 |
DEG_ODPH_VHL_1 | 288 | 301 | PF01847 | 0.570 |
DEG_SIAH_1 | 58 | 66 | PF03145 | 0.378 |
DOC_CKS1_1 | 174 | 179 | PF01111 | 0.552 |
DOC_MAPK_MEF2A_6 | 40 | 48 | PF00069 | 0.584 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.472 |
DOC_PP4_FxxP_1 | 355 | 358 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.708 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.726 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.463 |
LIG_Actin_WH2_2 | 176 | 192 | PF00022 | 0.523 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.546 |
LIG_deltaCOP1_diTrp_1 | 146 | 152 | PF00928 | 0.613 |
LIG_eIF4E_1 | 208 | 214 | PF01652 | 0.453 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.462 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.460 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.559 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.730 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.688 |
LIG_Integrin_isoDGR_2 | 348 | 350 | PF01839 | 0.508 |
LIG_LIR_Apic_2 | 266 | 272 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 354 | 358 | PF02991 | 0.538 |
LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.651 |
LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.453 |
LIG_MYND_3 | 255 | 259 | PF01753 | 0.612 |
LIG_Pex14_2 | 387 | 391 | PF04695 | 0.658 |
LIG_Rb_LxCxE_1 | 333 | 354 | PF01857 | 0.603 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.450 |
LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.492 |
LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.724 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.520 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.593 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.709 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.475 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.615 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.636 |
LIG_TRFH_1 | 286 | 290 | PF08558 | 0.471 |
LIG_WW_1 | 290 | 293 | PF00397 | 0.567 |
MOD_CDK_SPK_2 | 194 | 199 | PF00069 | 0.521 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.583 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.604 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.571 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.626 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.655 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.493 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.758 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.523 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.601 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.656 |
MOD_CMANNOS | 149 | 152 | PF00535 | 0.626 |
MOD_Cter_Amidation | 348 | 351 | PF01082 | 0.595 |
MOD_DYRK1A_RPxSP_1 | 173 | 177 | PF00069 | 0.585 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.698 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.687 |
MOD_GlcNHglycan | 182 | 186 | PF01048 | 0.444 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.552 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.624 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.562 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.699 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.764 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.370 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.454 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.402 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.537 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.488 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.488 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.689 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.475 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.522 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.690 |
MOD_NEK2_2 | 185 | 190 | PF00069 | 0.595 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.786 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.759 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.726 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.558 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.419 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.475 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.409 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.464 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.594 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.635 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.638 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.527 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.489 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.736 |
MOD_SUMO_rev_2 | 91 | 98 | PF00179 | 0.685 |
TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 350 | 354 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIQ0 | Leptomonas seymouri | 49% | 100% |
A4HYN2 | Leishmania infantum | 99% | 100% |
E9AI97 | Leishmania braziliensis | 73% | 100% |
E9AUI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QD02 | Leishmania major | 93% | 100% |