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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: A4H855
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.614 |
CLV_MEL_PAP_1 | 299 | 305 | PF00089 | 0.654 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.782 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.661 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.782 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.514 |
DEG_SCF_FBW7_1 | 156 | 162 | PF00400 | 0.584 |
DEG_SPOP_SBC_1 | 230 | 234 | PF00917 | 0.608 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.621 |
DOC_CDC14_PxL_1 | 420 | 428 | PF14671 | 0.652 |
DOC_CKS1_1 | 156 | 161 | PF01111 | 0.584 |
DOC_CKS1_1 | 184 | 189 | PF01111 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 54 | 60 | PF00134 | 0.698 |
DOC_MAPK_DCC_7 | 183 | 192 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 321 | 330 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 183 | 192 | PF00069 | 0.606 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.629 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.673 |
DOC_PP4_FxxP_1 | 82 | 85 | PF00568 | 0.812 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.613 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 117 | 124 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 223 | 230 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 381 | 386 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.675 |
LIG_APCC_ABBAyCdc20_2 | 400 | 406 | PF00400 | 0.711 |
LIG_BIR_III_2 | 338 | 342 | PF00653 | 0.744 |
LIG_BRCT_BRCA1_1 | 61 | 65 | PF00533 | 0.681 |
LIG_deltaCOP1_diTrp_1 | 354 | 361 | PF00928 | 0.565 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.630 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.607 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.610 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.718 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.624 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.608 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 42 | 47 | PF02991 | 0.662 |
LIG_LIR_Apic_2 | 80 | 85 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 137 | 145 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.566 |
LIG_Pex14_1 | 61 | 65 | PF04695 | 0.681 |
LIG_REV1ctd_RIR_1 | 174 | 180 | PF16727 | 0.613 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.679 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.582 |
LIG_SH2_SRC | 44 | 47 | PF00017 | 0.725 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.582 |
LIG_SH2_STAT3 | 344 | 347 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.745 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.559 |
LIG_SH3_2 | 316 | 321 | PF14604 | 0.554 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.568 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.638 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.784 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.744 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.806 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.607 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.828 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.505 |
LIG_TRFH_1 | 72 | 76 | PF08558 | 0.572 |
LIG_UBA3_1 | 393 | 400 | PF00899 | 0.458 |
LIG_WW_1 | 341 | 344 | PF00397 | 0.590 |
LIG_WW_3 | 315 | 319 | PF00397 | 0.704 |
MOD_CDC14_SPxK_1 | 315 | 318 | PF00782 | 0.699 |
MOD_CDK_SPxK_1 | 27 | 33 | PF00069 | 0.576 |
MOD_CDK_SPxK_1 | 312 | 318 | PF00069 | 0.688 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.806 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.506 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.746 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.604 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.811 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.616 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.507 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.508 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.662 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.666 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.680 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.830 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.663 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.499 |
MOD_DYRK1A_RPxSP_1 | 183 | 187 | PF00069 | 0.593 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.835 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.675 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.611 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.699 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.746 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.732 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.595 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.657 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.802 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.594 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.662 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.454 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.779 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.733 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.581 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.632 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.658 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.653 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.607 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.674 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.624 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.580 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.656 |
MOD_PKA_1 | 117 | 123 | PF00069 | 0.780 |
MOD_PKA_1 | 359 | 365 | PF00069 | 0.504 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.771 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.609 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.587 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.659 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.723 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.711 |
MOD_PKB_1 | 6 | 14 | PF00069 | 0.756 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.753 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.511 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.621 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.765 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.543 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.485 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.723 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.534 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.641 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.655 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.622 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.558 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.742 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.590 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.655 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.607 |
MOD_SUMO_rev_2 | 397 | 402 | PF00179 | 0.686 |
TRG_DiLeu_BaLyEn_6 | 389 | 394 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 421 | 426 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.712 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.714 |
TRG_ER_diArg_1 | 5 | 8 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WTN4 | Leishmania donovani | 64% | 99% |
A4HWI0 | Leishmania infantum | 63% | 99% |
E9AQ81 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |