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: 22 |
NetGPI | no | yes: 0, no: 23 |
Related structures:
AlphaFold database: Q4QGJ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 365 | 369 | PF00656 | 0.700 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.786 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.535 |
CLV_PCSK_FUR_1 | 393 | 397 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.638 |
CLV_Separin_Metazoa | 226 | 230 | PF03568 | 0.551 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.619 |
DOC_CYCLIN_RxL_1 | 392 | 402 | PF00134 | 0.655 |
DOC_MAPK_gen_1 | 319 | 327 | PF00069 | 0.708 |
DOC_MAPK_gen_1 | 34 | 44 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 8 | 18 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 11 | 18 | PF00069 | 0.570 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.601 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.664 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 30 | 34 | PF00244 | 0.791 |
LIG_14-3-3_CanoR_1 | 431 | 440 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 471 | 476 | PF00244 | 0.546 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.686 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.643 |
LIG_Clathr_ClatBox_1 | 130 | 134 | PF01394 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 310 | 315 | PF00928 | 0.582 |
LIG_EVH1_1 | 148 | 152 | PF00568 | 0.602 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.596 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.611 |
LIG_LIR_Apic_2 | 146 | 151 | PF02991 | 0.600 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.621 |
LIG_LIR_Apic_2 | 298 | 303 | PF02991 | 0.605 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.542 |
LIG_LIR_Apic_2 | 93 | 97 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 289 | 300 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.566 |
LIG_PCNA_PIPBox_1 | 116 | 125 | PF02747 | 0.698 |
LIG_PDZ_Wminus1_1 | 480 | 482 | PF00595 | 0.534 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.685 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.570 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.567 |
LIG_SH2_NCK_1 | 292 | 296 | PF00017 | 0.601 |
LIG_SH2_NCK_1 | 364 | 368 | PF00017 | 0.710 |
LIG_SH2_PTP2 | 300 | 303 | PF00017 | 0.612 |
LIG_SH2_SRC | 300 | 303 | PF00017 | 0.612 |
LIG_SH2_SRC | 364 | 367 | PF00017 | 0.673 |
LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.684 |
LIG_SH2_STAT3 | 70 | 73 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.565 |
LIG_SH3_1 | 420 | 426 | PF00018 | 0.733 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.587 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.598 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.594 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.611 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.625 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.658 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.748 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.623 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.628 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.717 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.654 |
LIG_WW_2 | 425 | 428 | PF00397 | 0.710 |
MOD_CDC14_SPxK_1 | 106 | 109 | PF00782 | 0.580 |
MOD_CDK_SPK_2 | 352 | 357 | PF00069 | 0.643 |
MOD_CDK_SPxK_1 | 103 | 109 | PF00069 | 0.581 |
MOD_CDK_SPxxK_3 | 10 | 17 | PF00069 | 0.569 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.724 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.577 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.568 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.588 |
MOD_Cter_Amidation | 305 | 308 | PF01082 | 0.722 |
MOD_Cter_Amidation | 317 | 320 | PF01082 | 0.529 |
MOD_GlcNHglycan | 23 | 29 | PF01048 | 0.767 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.678 |
MOD_GlcNHglycan | 400 | 404 | PF01048 | 0.663 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.652 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.721 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.786 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.687 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.559 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.695 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.752 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.573 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.579 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.625 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.581 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.717 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.687 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.752 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.581 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.513 |
MOD_Plk_2-3 | 452 | 458 | PF00069 | 0.588 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.554 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.581 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.643 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.559 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.573 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.570 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.567 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 258 | 261 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 475 | 478 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 395 | 400 | PF00026 | 0.662 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9T4 | Leptomonas seymouri | 79% | 100% |
A0A0S4IRN8 | Bodo saltans | 72% | 100% |
A0A1X0NP12 | Trypanosomatidae | 72% | 100% |
A0A381ME06 | Leishmania infantum | 95% | 100% |
A0A3Q8IHT5 | Leishmania donovani | 95% | 100% |
A0A3S7WS51 | Leishmania donovani | 95% | 100% |
A4H6Y7 | Leishmania braziliensis | 82% | 100% |
C9ZHZ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 72% | 100% |
E9AGG3 | Leishmania infantum | 95% | 100% |
E9AGG8 | Leishmania infantum | 95% | 100% |
E9AP06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QGI1 | Leishmania major | 98% | 100% |
Q4QGI3 | Leishmania major | 98% | 100% |
Q4QGJ5 | Leishmania major | 98% | 100% |
Q4QGJ8 | Leishmania major | 98% | 100% |
Q4QGK3 | Leishmania major | 99% | 83% |
Q4QGK5 | Leishmania major | 99% | 100% |
Q4QGK7 | Leishmania major | 99% | 100% |
Q4QGL3 | Leishmania major | 99% | 100% |
Q4QGL6 | Leishmania major | 98% | 100% |
Q4QGM0 | Leishmania major | 99% | 100% |
V5BF60 | Trypanosoma cruzi | 72% | 98% |