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: Q4QGI3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 318 | 322 | PF00656 | 0.693 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.788 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.528 |
CLV_PCSK_FUR_1 | 346 | 350 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.651 |
CLV_Separin_Metazoa | 179 | 183 | PF03568 | 0.574 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.435 |
DOC_CYCLIN_RxL_1 | 345 | 355 | PF00134 | 0.658 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.727 |
DOC_PP4_FxxP_1 | 101 | 104 | PF00568 | 0.602 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 384 | 393 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.545 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.706 |
LIG_Clathr_ClatBox_1 | 83 | 87 | PF01394 | 0.531 |
LIG_deltaCOP1_diTrp_1 | 263 | 268 | PF00928 | 0.653 |
LIG_EVH1_1 | 101 | 105 | PF00568 | 0.605 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.616 |
LIG_LIR_Apic_2 | 12 | 18 | PF02991 | 0.590 |
LIG_LIR_Apic_2 | 203 | 208 | PF02991 | 0.642 |
LIG_LIR_Apic_2 | 251 | 256 | PF02991 | 0.644 |
LIG_LIR_Apic_2 | 46 | 50 | PF02991 | 0.583 |
LIG_LIR_Apic_2 | 99 | 104 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 189 | 200 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 242 | 253 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.597 |
LIG_PCNA_PIPBox_1 | 69 | 78 | PF02747 | 0.683 |
LIG_PDZ_Wminus1_1 | 433 | 435 | PF00595 | 0.531 |
LIG_Pex14_2 | 280 | 284 | PF04695 | 0.747 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.617 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.600 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.646 |
LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.753 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.699 |
LIG_SH2_PTP2 | 253 | 256 | PF00017 | 0.645 |
LIG_SH2_SRC | 253 | 256 | PF00017 | 0.664 |
LIG_SH2_SRC | 317 | 320 | PF00017 | 0.668 |
LIG_SH2_STAT3 | 163 | 166 | PF00017 | 0.706 |
LIG_SH2_STAT3 | 23 | 26 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.585 |
LIG_SH3_1 | 373 | 379 | PF00018 | 0.733 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.612 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.628 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.642 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.674 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.726 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.601 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.605 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.649 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.679 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.733 |
LIG_WW_2 | 378 | 381 | PF00397 | 0.809 |
MOD_CDC14_SPxK_1 | 59 | 62 | PF00782 | 0.554 |
MOD_CDK_SPxK_1 | 56 | 62 | PF00069 | 0.572 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.799 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.577 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.545 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.735 |
MOD_Cter_Amidation | 258 | 261 | PF01082 | 0.735 |
MOD_Cter_Amidation | 270 | 273 | PF01082 | 0.698 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.698 |
MOD_GlcNHglycan | 353 | 357 | PF01048 | 0.639 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.629 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.581 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.763 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.790 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.768 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.669 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.575 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.622 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.602 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.594 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.751 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.592 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.517 |
MOD_Plk_2-3 | 405 | 411 | PF00069 | 0.589 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.590 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 428 | 431 | PF00400 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 348 | 353 | PF00026 | 0.660 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9T4 | Leptomonas seymouri | 79% | 98% |
A0A0S4IRN8 | Bodo saltans | 74% | 100% |
A0A1X0NP12 | Trypanosomatidae | 72% | 100% |
A0A381ME06 | Leishmania infantum | 94% | 99% |
A0A3Q8IHT5 | Leishmania donovani | 94% | 99% |
A0A3S7WS51 | Leishmania donovani | 94% | 99% |
A4H6Y7 | Leishmania braziliensis | 82% | 99% |
C9ZHZ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 100% |
E9AGG3 | Leishmania infantum | 94% | 99% |
E9AGG8 | Leishmania infantum | 94% | 99% |
E9AP06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q4QGI1 | Leishmania major | 97% | 100% |
Q4QGJ1 | Leishmania major | 100% | 100% |
Q4QGJ3 | Leishmania major | 98% | 90% |
Q4QGJ5 | Leishmania major | 98% | 91% |
Q4QGJ8 | Leishmania major | 99% | 90% |
Q4QGK3 | Leishmania major | 99% | 74% |
Q4QGK5 | Leishmania major | 99% | 90% |
Q4QGK7 | Leishmania major | 99% | 90% |
Q4QGL3 | Leishmania major | 99% | 90% |
Q4QGL6 | Leishmania major | 99% | 95% |
Q4QGM0 | Leishmania major | 99% | 90% |
V5BF60 | Trypanosoma cruzi | 73% | 88% |