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: E9B6W8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.676 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.763 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.758 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.763 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.564 |
CLV_Separin_Metazoa | 183 | 187 | PF03568 | 0.686 |
CLV_Separin_Metazoa | 268 | 272 | PF03568 | 0.725 |
CLV_Separin_Metazoa | 353 | 357 | PF03568 | 0.627 |
CLV_Separin_Metazoa | 68 | 72 | PF03568 | 0.712 |
CLV_Separin_Metazoa | 98 | 102 | PF03568 | 0.688 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.751 |
DEG_SPOP_SBC_1 | 226 | 230 | PF00917 | 0.746 |
DEG_SPOP_SBC_1 | 311 | 315 | PF00917 | 0.703 |
DOC_CKS1_1 | 534 | 539 | PF01111 | 0.817 |
DOC_MAPK_MEF2A_6 | 526 | 534 | PF00069 | 0.741 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.591 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.752 |
DOC_USP7_UBL2_3 | 102 | 106 | PF12436 | 0.732 |
DOC_USP7_UBL2_3 | 107 | 111 | PF12436 | 0.695 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.778 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.689 |
DOC_USP7_UBL2_3 | 187 | 191 | PF12436 | 0.732 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.709 |
DOC_USP7_UBL2_3 | 238 | 242 | PF12436 | 0.845 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.723 |
DOC_USP7_UBL2_3 | 272 | 276 | PF12436 | 0.748 |
DOC_USP7_UBL2_3 | 277 | 281 | PF12436 | 0.719 |
DOC_USP7_UBL2_3 | 323 | 327 | PF12436 | 0.761 |
DOC_USP7_UBL2_3 | 332 | 336 | PF12436 | 0.694 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.674 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 385 | 389 | PF12436 | 0.557 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.704 |
DOC_USP7_UBL2_3 | 77 | 81 | PF12436 | 0.662 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 533 | 538 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.742 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 542 | 547 | PF00244 | 0.661 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.640 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.575 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.814 |
LIG_SH2_NCK_1 | 23 | 27 | PF00017 | 0.629 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.529 |
LIG_SH3_1 | 366 | 372 | PF00018 | 0.586 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.810 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.803 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.811 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.802 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.825 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.817 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.795 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.787 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.814 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.685 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.660 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.812 |
LIG_SH3_4 | 102 | 109 | PF00018 | 0.777 |
LIG_SH3_4 | 153 | 160 | PF00018 | 0.815 |
LIG_SH3_4 | 162 | 169 | PF00018 | 0.696 |
LIG_SH3_4 | 187 | 194 | PF00018 | 0.777 |
LIG_SH3_4 | 238 | 245 | PF00018 | 0.754 |
LIG_SH3_4 | 247 | 254 | PF00018 | 0.644 |
LIG_SH3_4 | 272 | 279 | PF00018 | 0.833 |
LIG_SH3_4 | 323 | 330 | PF00018 | 0.700 |
LIG_SH3_4 | 332 | 339 | PF00018 | 0.617 |
LIG_SH3_4 | 357 | 364 | PF00018 | 0.613 |
LIG_SH3_4 | 385 | 392 | PF00018 | 0.560 |
LIG_SH3_4 | 72 | 79 | PF00018 | 0.830 |
LIG_TRAF2_1 | 29 | 32 | PF00917 | 0.564 |
MOD_CDK_SPK_2 | 106 | 111 | PF00069 | 0.677 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.750 |
MOD_CDK_SPK_2 | 191 | 196 | PF00069 | 0.683 |
MOD_CDK_SPK_2 | 242 | 247 | PF00069 | 0.756 |
MOD_CDK_SPK_2 | 276 | 281 | PF00069 | 0.710 |
MOD_CDK_SPK_2 | 327 | 332 | PF00069 | 0.704 |
MOD_CDK_SPK_2 | 361 | 366 | PF00069 | 0.669 |
MOD_CDK_SPK_2 | 76 | 81 | PF00069 | 0.742 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.528 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.749 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.632 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.731 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.744 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.741 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.699 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.669 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.767 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.547 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.564 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.573 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.734 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.584 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.732 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.691 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.579 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.843 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.640 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.809 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.627 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.797 |
MOD_N-GLC_1 | 542 | 547 | PF02516 | 0.715 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.502 |
MOD_PK_1 | 542 | 548 | PF00069 | 0.646 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.523 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.716 |
MOD_Plk_2-3 | 121 | 127 | PF00069 | 0.677 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.713 |
MOD_Plk_2-3 | 176 | 182 | PF00069 | 0.738 |
MOD_Plk_2-3 | 206 | 212 | PF00069 | 0.709 |
MOD_Plk_2-3 | 227 | 233 | PF00069 | 0.746 |
MOD_Plk_2-3 | 261 | 267 | PF00069 | 0.722 |
MOD_Plk_2-3 | 291 | 297 | PF00069 | 0.684 |
MOD_Plk_2-3 | 312 | 318 | PF00069 | 0.697 |
MOD_Plk_2-3 | 346 | 352 | PF00069 | 0.739 |
MOD_Plk_2-3 | 61 | 67 | PF00069 | 0.617 |
MOD_Plk_2-3 | 91 | 97 | PF00069 | 0.741 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.678 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.750 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.705 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.684 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.754 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.607 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.710 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.703 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.716 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.670 |
MOD_ProDKin_1 | 533 | 539 | PF00069 | 0.722 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.742 |
MOD_SUMO_for_1 | 6 | 9 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 377 | 387 | PF00179 | 0.563 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X9Y7 | Leishmania donovani | 78% | 86% |
A4HNA7 | Leishmania braziliensis | 62% | 100% |
A4IBX8 | Leishmania infantum | 73% | 98% |
C9ZYM9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 99% |
E9AFR5 | Leishmania major | 64% | 100% |