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: 23 |
NetGPI | no | yes: 0, no: 24 |
Related structures:
AlphaFold database: E9AP06
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 365 | 369 | PF00656 | 0.721 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.656 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.740 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.676 |
CLV_Separin_Metazoa | 226 | 230 | PF03568 | 0.604 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.644 |
DOC_CYCLIN_RxL_1 | 392 | 402 | PF00134 | 0.684 |
DOC_MAPK_gen_1 | 319 | 327 | PF00069 | 0.733 |
DOC_MAPK_gen_1 | 34 | 44 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 8 | 18 | PF00069 | 0.659 |
DOC_MAPK_MEF2A_6 | 11 | 18 | PF00069 | 0.610 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.576 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.711 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 312 | 321 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 431 | 435 | PF00244 | 0.766 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.653 |
LIG_deltaCOP1_diTrp_1 | 310 | 315 | PF00928 | 0.643 |
LIG_EVH1_1 | 148 | 152 | PF00568 | 0.576 |
LIG_EVH1_2 | 29 | 33 | PF00568 | 0.497 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.634 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.614 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.578 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.690 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.406 |
LIG_LIR_Apic_2 | 146 | 151 | PF02991 | 0.587 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.645 |
LIG_LIR_Apic_2 | 299 | 303 | PF02991 | 0.645 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.563 |
LIG_LIR_Apic_2 | 93 | 97 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 175 | 181 | PF02991 | 0.743 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 289 | 300 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.580 |
LIG_PCNA_PIPBox_1 | 116 | 125 | PF02747 | 0.654 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.723 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.622 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.581 |
LIG_SH2_NCK_1 | 292 | 296 | PF00017 | 0.651 |
LIG_SH2_PTP2 | 300 | 303 | PF00017 | 0.645 |
LIG_SH2_SRC | 300 | 303 | PF00017 | 0.665 |
LIG_SH2_SRC | 364 | 367 | PF00017 | 0.699 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.524 |
LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.751 |
LIG_SH2_STAT3 | 70 | 73 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.599 |
LIG_SH3_1 | 420 | 426 | PF00018 | 0.753 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.596 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.583 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.596 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.634 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.459 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.650 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.697 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.746 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.651 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.675 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.737 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.666 |
LIG_UBA3_1 | 130 | 134 | PF00899 | 0.557 |
LIG_WW_2 | 425 | 428 | PF00397 | 0.831 |
MOD_CDC14_SPxK_1 | 106 | 109 | PF00782 | 0.562 |
MOD_CDK_SPK_2 | 352 | 357 | PF00069 | 0.670 |
MOD_CDK_SPxK_1 | 103 | 109 | PF00069 | 0.574 |
MOD_CDK_SPxxK_3 | 10 | 17 | PF00069 | 0.603 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.814 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.571 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.474 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.565 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.613 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.402 |
MOD_Cter_Amidation | 305 | 308 | PF01082 | 0.739 |
MOD_Cter_Amidation | 317 | 320 | PF01082 | 0.716 |
MOD_DYRK1A_RPxSP_1 | 431 | 435 | PF00069 | 0.522 |
MOD_GlcNHglycan | 23 | 29 | PF01048 | 0.751 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.715 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.478 |
MOD_GlcNHglycan | 400 | 404 | PF01048 | 0.664 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.650 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.790 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.567 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.785 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.695 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.612 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.578 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.453 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.633 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.574 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.626 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.597 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.438 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.474 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.741 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.585 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.538 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.580 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.574 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.668 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.598 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.577 |
TRG_DiLeu_BaEn_4 | 223 | 229 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.603 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.578 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 258 | 261 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 395 | 400 | PF00026 | 0.685 |
TRG_PTS2 | 1 | 48 | PF00400 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9T4 | Leptomonas seymouri | 84% | 99% |
A0A0S4IRN8 | Bodo saltans | 76% | 100% |
A0A1X0NP12 | Trypanosomatidae | 76% | 100% |
A0A381ME06 | Leishmania infantum | 94% | 100% |
A0A3Q8IHT5 | Leishmania donovani | 94% | 100% |
A0A3S7WS51 | Leishmania donovani | 94% | 100% |
A4H6Y7 | Leishmania braziliensis | 86% | 100% |
C9ZHZ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 77% | 100% |
E9AGG3 | Leishmania infantum | 94% | 100% |
E9AGG8 | Leishmania infantum | 94% | 100% |
Q4QGI1 | Leishmania major | 93% | 100% |
Q4QGI3 | Leishmania major | 91% | 100% |
Q4QGJ1 | Leishmania major | 95% | 100% |
Q4QGJ3 | Leishmania major | 92% | 100% |
Q4QGJ5 | Leishmania major | 91% | 100% |
Q4QGJ8 | Leishmania major | 92% | 100% |
Q4QGK3 | Leishmania major | 92% | 100% |
Q4QGK5 | Leishmania major | 92% | 100% |
Q4QGK7 | Leishmania major | 93% | 100% |
Q4QGL3 | Leishmania major | 92% | 100% |
Q4QGL6 | Leishmania major | 91% | 100% |
Q4QGM0 | Leishmania major | 91% | 100% |
V5BF60 | Trypanosoma cruzi | 77% | 89% |