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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3Q8IB32
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 8 |
GO:0005515 | protein binding | 2 | 8 |
GO:0051087 | protein-folding chaperone binding | 3 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.470 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.268 |
CLV_PCSK_FUR_1 | 432 | 436 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.273 |
CLV_Separin_Metazoa | 413 | 417 | PF03568 | 0.448 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.351 |
DEG_SCF_FBW7_1 | 74 | 81 | PF00400 | 0.401 |
DOC_CKS1_1 | 75 | 80 | PF01111 | 0.488 |
DOC_CYCLIN_RxL_1 | 413 | 422 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 16 | 25 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 295 | 302 | PF00069 | 0.618 |
DOC_MAPK_MEF2A_6 | 19 | 27 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 295 | 302 | PF00069 | 0.580 |
DOC_PP1_RVXF_1 | 414 | 420 | PF00149 | 0.448 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.424 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.398 |
DOC_USP7_UBL2_3 | 169 | 173 | PF12436 | 0.691 |
DOC_USP7_UBL2_3 | 436 | 440 | PF12436 | 0.516 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 130 | 139 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 163 | 168 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 85 | 89 | PF00244 | 0.655 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.568 |
LIG_BIR_III_4 | 447 | 451 | PF00653 | 0.463 |
LIG_eIF4E_1 | 68 | 74 | PF01652 | 0.490 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.609 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.826 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.434 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.394 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.448 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.267 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.636 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.554 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.395 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.449 |
LIG_GBD_Chelix_1 | 32 | 40 | PF00786 | 0.445 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.448 |
LIG_MYND_1 | 335 | 339 | PF01753 | 0.485 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 141 | 145 | PF00017 | 0.622 |
LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.622 |
LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.448 |
LIG_SH2_STAT3 | 4 | 7 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.422 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.677 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.623 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.695 |
LIG_SH3_4 | 338 | 345 | PF00018 | 0.409 |
LIG_SUMO_SIM_anti_2 | 380 | 386 | PF11976 | 0.431 |
LIG_SUMO_SIM_anti_2 | 389 | 395 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 348 | 353 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 383 | 390 | PF11976 | 0.344 |
LIG_TRAF2_2 | 261 | 266 | PF00917 | 0.631 |
LIG_TYR_ITIM | 52 | 57 | PF00017 | 0.471 |
LIG_WRC_WIRS_1 | 36 | 41 | PF05994 | 0.420 |
LIG_WW_3 | 88 | 92 | PF00397 | 0.653 |
MOD_CDK_SPK_2 | 267 | 272 | PF00069 | 0.802 |
MOD_CDK_SPK_2 | 350 | 355 | PF00069 | 0.365 |
MOD_CDK_SPxxK_3 | 350 | 357 | PF00069 | 0.435 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.786 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.706 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.714 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.729 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.480 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.516 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.664 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.470 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.599 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.381 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.632 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.504 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.700 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.673 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.621 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.715 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.707 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.689 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.512 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.677 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.619 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.623 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.603 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.541 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.619 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.554 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.631 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.702 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.566 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.489 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.646 |
MOD_PK_1 | 348 | 354 | PF00069 | 0.317 |
MOD_PKA_1 | 162 | 168 | PF00069 | 0.693 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.790 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.519 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.490 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.797 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.589 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.371 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.415 |
MOD_Plk_2-3 | 380 | 386 | PF00069 | 0.402 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.599 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.417 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.375 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.570 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.650 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.688 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.530 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.690 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.807 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.454 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.348 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.496 |
MOD_SUMO_rev_2 | 447 | 456 | PF00179 | 0.637 |
TRG_DiLeu_BaEn_1 | 380 | 385 | PF01217 | 0.434 |
TRG_DiLeu_BaEn_2 | 34 | 40 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_3 | 412 | 418 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G1 | Leptomonas seymouri | 50% | 96% |
A4HC67 | Leishmania braziliensis | 69% | 100% |
A4HZP2 | Leishmania infantum | 100% | 100% |
C9ZSD2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AVJ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QBY1 | Leishmania major | 91% | 100% |
V5BK86 | Trypanosoma cruzi | 33% | 98% |