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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QB66
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.669 |
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.712 |
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.636 |
CLV_PCSK_FUR_1 | 289 | 293 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.805 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 290 | 292 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.764 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.459 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.665 |
DEG_SPOP_SBC_1 | 322 | 326 | PF00917 | 0.616 |
DOC_MAPK_gen_1 | 254 | 261 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 289 | 296 | PF00069 | 0.560 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.520 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 172 | 176 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 377 | 385 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 6 | 16 | PF00244 | 0.622 |
LIG_BIR_III_2 | 92 | 96 | PF00653 | 0.525 |
LIG_BIR_III_4 | 186 | 190 | PF00653 | 0.524 |
LIG_BIR_III_4 | 335 | 339 | PF00653 | 0.704 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.768 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.455 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.698 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.456 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.696 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.664 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.510 |
LIG_Integrin_RGD_1 | 345 | 347 | PF01839 | 0.693 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.508 |
LIG_LYPXL_SIV_4 | 41 | 49 | PF13949 | 0.467 |
LIG_NRBOX | 67 | 73 | PF00104 | 0.499 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.702 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.444 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 38 | 42 | PF00017 | 0.520 |
LIG_SH2_PTP2 | 42 | 45 | PF00017 | 0.470 |
LIG_SH2_SRC | 42 | 45 | PF00017 | 0.470 |
LIG_SH2_SRC | 64 | 67 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.706 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.486 |
LIG_SUMO_SIM_anti_2 | 257 | 264 | PF11976 | 0.500 |
LIG_SUMO_SIM_anti_2 | 83 | 89 | PF11976 | 0.501 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.510 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.584 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.695 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.440 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.541 |
MOD_CDK_SPxK_1 | 301 | 307 | PF00069 | 0.648 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.621 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.669 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.455 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.557 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.513 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.563 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.705 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.612 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.482 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.579 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.469 |
MOD_Cter_Amidation | 337 | 340 | PF01082 | 0.754 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.772 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.649 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.436 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.621 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.582 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.798 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.593 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.660 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.656 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.429 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.526 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.698 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.724 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.783 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.693 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.517 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.656 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.341 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.504 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.478 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.563 |
MOD_PK_1 | 284 | 290 | PF00069 | 0.517 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.736 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.651 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.736 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.647 |
MOD_Plk_2-3 | 105 | 111 | PF00069 | 0.755 |
MOD_Plk_2-3 | 129 | 135 | PF00069 | 0.680 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.553 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.593 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.589 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.455 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.705 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.681 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.625 |
TRG_DiLeu_BaEn_1 | 257 | 262 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_2 | 85 | 91 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.653 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.699 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.801 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.581 |
TRG_NLS_MonoCore_2 | 288 | 293 | PF00514 | 0.543 |
TRG_NLS_MonoExtN_4 | 289 | 294 | PF00514 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 235 | 240 | PF00026 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 292 | 297 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDP9 | Leptomonas seymouri | 52% | 100% |
A0A3S5H7C1 | Leishmania donovani | 89% | 99% |
A4HCW6 | Leishmania braziliensis | 74% | 100% |
A4I0E6 | Leishmania infantum | 90% | 100% |
E9AWA9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |