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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A4H3G9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.756 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.805 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.756 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.805 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.592 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.602 |
DOC_MAPK_DCC_7 | 234 | 243 | PF00069 | 0.640 |
DOC_MAPK_MEF2A_6 | 234 | 243 | PF00069 | 0.640 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.657 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.606 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.712 |
LIG_AP2alpha_2 | 347 | 349 | PF02296 | 0.776 |
LIG_APCC_ABBA_1 | 215 | 220 | PF00400 | 0.564 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.649 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.897 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.638 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.583 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.664 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.643 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.662 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.720 |
LIG_IBAR_NPY_1 | 255 | 257 | PF08397 | 0.620 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.674 |
LIG_LIR_Apic_2 | 7 | 11 | PF02991 | 0.765 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 283 | 288 | PF02991 | 0.658 |
LIG_PTAP_UEV_1 | 336 | 341 | PF05743 | 0.890 |
LIG_SH2_GRB2like | 31 | 34 | PF00017 | 0.706 |
LIG_SH2_NCK_1 | 170 | 174 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.612 |
LIG_SH3_2 | 331 | 336 | PF14604 | 0.905 |
LIG_SH3_2 | 341 | 346 | PF14604 | 0.642 |
LIG_SH3_2 | 424 | 429 | PF14604 | 0.673 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.635 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.582 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.553 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.330 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.716 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.466 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.601 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.723 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.797 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.629 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.606 |
LIG_TRAF2_1 | 361 | 364 | PF00917 | 0.837 |
MOD_CDC14_SPxK_1 | 426 | 429 | PF00782 | 0.634 |
MOD_CDK_SPK_2 | 264 | 269 | PF00069 | 0.391 |
MOD_CDK_SPK_2 | 423 | 428 | PF00069 | 0.629 |
MOD_CDK_SPK_2 | 50 | 55 | PF00069 | 0.724 |
MOD_CDK_SPxK_1 | 423 | 429 | PF00069 | 0.673 |
MOD_CDK_SPxK_1 | 50 | 56 | PF00069 | 0.731 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.615 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.731 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.675 |
MOD_Cter_Amidation | 409 | 412 | PF01082 | 0.623 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.695 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.294 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.736 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.692 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.656 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.711 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.363 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.888 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.656 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.654 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.648 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.711 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.614 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.654 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.677 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.709 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.664 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.857 |
MOD_PKA_1 | 419 | 425 | PF00069 | 0.635 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.903 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.417 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.644 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.682 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.651 |
MOD_Plk_2-3 | 301 | 307 | PF00069 | 0.675 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.688 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.612 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.641 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.651 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.623 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.388 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.666 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.731 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.624 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.738 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4H3G2 | Leishmania braziliensis | 96% | 100% |