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: Q4QJ33
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.741 |
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.713 |
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.773 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.747 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.781 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.769 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.769 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.616 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.791 |
DEG_SPOP_SBC_1 | 264 | 268 | PF00917 | 0.722 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.708 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.807 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.624 |
DOC_ANK_TNKS_1 | 452 | 459 | PF00023 | 0.646 |
DOC_CYCLIN_yClb1_LxF_4 | 256 | 261 | PF00134 | 0.612 |
DOC_MAPK_DCC_7 | 342 | 351 | PF00069 | 0.707 |
DOC_MAPK_gen_1 | 113 | 123 | PF00069 | 0.713 |
DOC_MAPK_gen_1 | 401 | 410 | PF00069 | 0.656 |
DOC_MAPK_MEF2A_6 | 219 | 226 | PF00069 | 0.795 |
DOC_MAPK_MEF2A_6 | 342 | 351 | PF00069 | 0.707 |
DOC_MAPK_MEF2A_6 | 376 | 384 | PF00069 | 0.544 |
DOC_MAPK_NFAT4_5 | 219 | 227 | PF00069 | 0.794 |
DOC_PP1_RVXF_1 | 256 | 262 | PF00149 | 0.615 |
DOC_PP4_FxxP_1 | 143 | 146 | PF00568 | 0.585 |
DOC_PP4_FxxP_1 | 18 | 21 | PF00568 | 0.727 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.685 |
DOC_USP7_UBL2_3 | 392 | 396 | PF12436 | 0.777 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 138 | 144 | PF00244 | 0.818 |
LIG_14-3-3_CanoR_1 | 16 | 21 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 271 | 277 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.637 |
LIG_Actin_WH2_2 | 256 | 273 | PF00022 | 0.575 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.725 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.678 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.710 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.782 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.658 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.572 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.775 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.727 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.694 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.734 |
LIG_LIR_Apic_2 | 141 | 146 | PF02991 | 0.583 |
LIG_LIR_Apic_2 | 15 | 21 | PF02991 | 0.726 |
LIG_LIR_Gen_1 | 75 | 82 | PF02991 | 0.812 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.759 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.813 |
LIG_SH2_CRK | 377 | 381 | PF00017 | 0.663 |
LIG_SH2_CRK | 43 | 47 | PF00017 | 0.725 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.727 |
LIG_SH2_GRB2like | 377 | 380 | PF00017 | 0.664 |
LIG_SH2_NCK_1 | 7 | 11 | PF00017 | 0.727 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.701 |
LIG_SH3_1 | 334 | 340 | PF00018 | 0.624 |
LIG_SH3_2 | 253 | 258 | PF14604 | 0.570 |
LIG_SH3_2 | 337 | 342 | PF14604 | 0.621 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.695 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.732 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.697 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.681 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.624 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.699 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.663 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.701 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.676 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.575 |
LIG_WW_3 | 93 | 97 | PF00397 | 0.707 |
MOD_CDC14_SPxK_1 | 268 | 271 | PF00782 | 0.806 |
MOD_CDK_SPxK_1 | 265 | 271 | PF00069 | 0.803 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.675 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.618 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.679 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.632 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.616 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.782 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.565 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.742 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.789 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.701 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.674 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.719 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.725 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.693 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.792 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.530 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.644 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.691 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.640 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.705 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.731 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.713 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.715 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.760 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.790 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.770 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.811 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.668 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.593 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.593 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.614 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.747 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.680 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.716 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.642 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.644 |
MOD_LATS_1 | 4 | 10 | PF00433 | 0.685 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.589 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.732 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.567 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.720 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.692 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.787 |
MOD_NEK2_2 | 347 | 352 | PF00069 | 0.576 |
MOD_PK_1 | 304 | 310 | PF00069 | 0.524 |
MOD_PK_1 | 6 | 12 | PF00069 | 0.707 |
MOD_PKA_1 | 304 | 310 | PF00069 | 0.602 |
MOD_PKA_1 | 328 | 334 | PF00069 | 0.580 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.726 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.750 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.659 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.770 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.604 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.709 |
MOD_PKB_1 | 302 | 310 | PF00069 | 0.530 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.740 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.714 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.579 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.703 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.703 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.705 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.718 |
TRG_DiLeu_BaEn_1 | 389 | 394 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.742 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.726 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.724 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.714 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3T5 | Leptomonas seymouri | 37% | 93% |
A0A3S5H5Q5 | Leishmania donovani | 82% | 100% |
A4H4L1 | Leishmania braziliensis | 50% | 91% |
A4HST7 | Leishmania infantum | 82% | 100% |
E9AKS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |