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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9B2I5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.583 |
CLV_PCSK_FUR_1 | 118 | 122 | PF00082 | 0.497 |
CLV_PCSK_FUR_1 | 182 | 186 | PF00082 | 0.718 |
CLV_PCSK_FUR_1 | 75 | 79 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.413 |
CLV_PCSK_PC7_1 | 180 | 186 | PF00082 | 0.719 |
CLV_PCSK_PC7_1 | 50 | 56 | PF00082 | 0.567 |
CLV_PCSK_PC7_1 | 73 | 79 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.448 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.645 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.549 |
DOC_CKS1_1 | 262 | 267 | PF01111 | 0.432 |
DOC_CYCLIN_RxL_1 | 37 | 46 | PF00134 | 0.458 |
DOC_CYCLIN_yCln2_LP_2 | 262 | 268 | PF00134 | 0.466 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.427 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.572 |
DOC_USP7_UBL2_3 | 22 | 26 | PF12436 | 0.461 |
DOC_USP7_UBL2_3 | 226 | 230 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 118 | 126 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.653 |
LIG_BIR_III_4 | 322 | 326 | PF00653 | 0.439 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.542 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.406 |
LIG_Integrin_RGD_1 | 105 | 107 | PF01839 | 0.578 |
LIG_Integrin_RGD_1 | 96 | 98 | PF01839 | 0.689 |
LIG_LIR_Gen_1 | 250 | 258 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 290 | 301 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.541 |
LIG_MLH1_MIPbox_1 | 369 | 373 | PF16413 | 0.496 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.620 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.586 |
LIG_SH2_PTP2 | 253 | 256 | PF00017 | 0.395 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.404 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.578 |
LIG_WRC_WIRS_1 | 369 | 374 | PF05994 | 0.501 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.629 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.356 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.424 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.570 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.645 |
MOD_Cter_Amidation | 91 | 94 | PF01082 | 0.714 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.572 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.684 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.426 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.728 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.591 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.614 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.608 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.645 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.620 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.421 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.405 |
MOD_LATS_1 | 20 | 26 | PF00433 | 0.438 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.468 |
MOD_NEK2_2 | 368 | 373 | PF00069 | 0.519 |
MOD_OFUCOSY | 255 | 261 | PF10250 | 0.396 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.593 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.409 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.385 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.437 |
MOD_PKA_1 | 221 | 227 | PF00069 | 0.460 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.543 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.732 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.571 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.525 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.483 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.585 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.688 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.573 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.711 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.577 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.448 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.462 |
TRG_AP2beta_CARGO_1 | 13 | 23 | PF09066 | 0.383 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.663 |
TRG_NLS_MonoExtC_3 | 21 | 26 | PF00514 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 40 | 44 | PF00026 | 0.518 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEL1 | Leptomonas seymouri | 56% | 97% |
A0A1X0NV62 | Trypanosomatidae | 31% | 100% |
A0A3Q8IFQ4 | Leishmania donovani | 94% | 99% |
A4HK42 | Leishmania braziliensis | 88% | 100% |
A4I7M0 | Leishmania infantum | 94% | 99% |
D0A9S8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4Q5M1 | Leishmania major | 92% | 100% |
V5BAR8 | Trypanosoma cruzi | 31% | 100% |