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: Q4QGJ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.705 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.800 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.536 |
CLV_PCSK_FUR_1 | 388 | 392 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.678 |
CLV_Separin_Metazoa | 226 | 230 | PF03568 | 0.583 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.617 |
DOC_CYCLIN_RxL_1 | 387 | 397 | PF00134 | 0.684 |
DOC_MAPK_gen_1 | 319 | 327 | PF00069 | 0.741 |
DOC_MAPK_gen_1 | 34 | 44 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 72 | 81 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 8 | 18 | PF00069 | 0.629 |
DOC_MAPK_MEF2A_6 | 11 | 18 | PF00069 | 0.588 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.689 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.561 |
LIG_14-3-3_CanoR_1 | 30 | 34 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 426 | 435 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 466 | 471 | PF00244 | 0.548 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.729 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.647 |
LIG_Clathr_ClatBox_1 | 130 | 134 | PF01394 | 0.492 |
LIG_deltaCOP1_diTrp_1 | 310 | 315 | PF00928 | 0.662 |
LIG_EVH1_1 | 148 | 152 | PF00568 | 0.573 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.613 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.627 |
LIG_LIR_Apic_2 | 146 | 151 | PF02991 | 0.591 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 298 | 303 | PF02991 | 0.646 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.552 |
LIG_LIR_Apic_2 | 93 | 97 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 289 | 300 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.570 |
LIG_PCNA_PIPBox_1 | 116 | 125 | PF02747 | 0.651 |
LIG_PDZ_Wminus1_1 | 475 | 477 | PF00595 | 0.535 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.762 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.601 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.566 |
LIG_SH2_NCK_1 | 292 | 296 | PF00017 | 0.631 |
LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.776 |
LIG_SH2_NCK_1 | 359 | 363 | PF00017 | 0.713 |
LIG_SH2_PTP2 | 300 | 303 | PF00017 | 0.657 |
LIG_SH2_SRC | 300 | 303 | PF00017 | 0.657 |
LIG_SH2_SRC | 359 | 362 | PF00017 | 0.682 |
LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.710 |
LIG_SH2_STAT3 | 70 | 73 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.584 |
LIG_SH3_1 | 415 | 421 | PF00018 | 0.753 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.592 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.581 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.591 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.625 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.656 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.693 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.739 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.643 |
LIG_TRAF2_1 | 223 | 226 | PF00917 | 0.658 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.731 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.663 |
LIG_WW_2 | 420 | 423 | PF00397 | 0.820 |
MOD_CDC14_SPxK_1 | 106 | 109 | PF00782 | 0.560 |
MOD_CDK_SPxK_1 | 103 | 109 | PF00069 | 0.576 |
MOD_CDK_SPxxK_3 | 10 | 17 | PF00069 | 0.584 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.806 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.589 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.600 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.593 |
MOD_Cter_Amidation | 305 | 308 | PF01082 | 0.739 |
MOD_Cter_Amidation | 317 | 320 | PF01082 | 0.561 |
MOD_GlcNHglycan | 23 | 29 | PF01048 | 0.717 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.748 |
MOD_GlcNHglycan | 395 | 399 | PF01048 | 0.692 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.676 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.773 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.799 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.819 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.553 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.698 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.736 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.583 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.630 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.646 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.582 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.732 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.698 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.766 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.589 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.554 |
MOD_Plk_2-3 | 447 | 453 | PF00069 | 0.593 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.567 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.576 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.590 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.589 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.567 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 258 | 261 | PF00400 | 0.729 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 470 | 473 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 390 | 395 | PF00026 | 0.685 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9T4 | Leptomonas seymouri | 79% | 100% |
A0A0S4IRN8 | Bodo saltans | 71% | 100% |
A0A1X0NP12 | Trypanosomatidae | 72% | 100% |
A0A381ME06 | Leishmania infantum | 94% | 100% |
A0A3Q8IHT5 | Leishmania donovani | 94% | 100% |
A0A3S7WS51 | Leishmania donovani | 94% | 100% |
A4H6Y7 | Leishmania braziliensis | 81% | 100% |
C9ZHZ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 72% | 100% |
E9AGG3 | Leishmania infantum | 94% | 100% |
E9AGG8 | Leishmania infantum | 94% | 100% |
E9AP06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QGI1 | Leishmania major | 97% | 100% |
Q4QGI3 | Leishmania major | 98% | 100% |
Q4QGJ3 | Leishmania major | 98% | 100% |
Q4QGJ8 | Leishmania major | 99% | 99% |
Q4QGK3 | Leishmania major | 98% | 82% |
Q4QGK5 | Leishmania major | 98% | 99% |
Q4QGK7 | Leishmania major | 99% | 99% |
Q4QGL3 | Leishmania major | 98% | 99% |
Q4QGL6 | Leishmania major | 98% | 100% |
Q4QGM0 | Leishmania major | 98% | 99% |
V5BF60 | Trypanosoma cruzi | 72% | 97% |