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: A4HC67
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005515 | protein binding | 2 | 7 |
GO:0051087 | protein-folding chaperone binding | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.759 |
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.782 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.346 |
CLV_PCSK_FUR_1 | 430 | 434 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.773 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.759 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.786 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.346 |
CLV_Separin_Metazoa | 411 | 415 | PF03568 | 0.546 |
DEG_SCF_TRCP1_1 | 358 | 363 | PF00400 | 0.349 |
DEG_SPOP_SBC_1 | 177 | 181 | PF00917 | 0.573 |
DOC_CKS1_1 | 207 | 212 | PF01111 | 0.548 |
DOC_CYCLIN_RxL_1 | 411 | 420 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 128 | 135 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 16 | 25 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 293 | 300 | PF00069 | 0.689 |
DOC_MAPK_MEF2A_6 | 19 | 27 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 293 | 300 | PF00069 | 0.684 |
DOC_MAPK_MEF2A_6 | 446 | 453 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 412 | 418 | PF00149 | 0.546 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.503 |
DOC_PP4_FxxP_1 | 197 | 200 | PF00568 | 0.574 |
DOC_PP4_FxxP_1 | 204 | 207 | PF00568 | 0.530 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.496 |
DOC_USP7_UBL2_3 | 167 | 171 | PF12436 | 0.811 |
DOC_USP7_UBL2_3 | 346 | 350 | PF12436 | 0.390 |
DOC_USP7_UBL2_3 | 434 | 438 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.825 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 169 | 178 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 184 | 191 | PF00244 | 0.629 |
LIG_Clathr_ClatBox_1 | 382 | 386 | PF01394 | 0.424 |
LIG_EH1_1 | 318 | 326 | PF00400 | 0.339 |
LIG_eIF4E_1 | 68 | 74 | PF01652 | 0.494 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.560 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.577 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.567 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.576 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.320 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.371 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.344 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.546 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.506 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.764 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.563 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.660 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.577 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.530 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.391 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.463 |
LIG_GBD_Chelix_1 | 32 | 40 | PF00786 | 0.570 |
LIG_LIR_Apic_2 | 195 | 200 | PF02991 | 0.642 |
LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.550 |
LIG_MYND_1 | 214 | 218 | PF01753 | 0.577 |
LIG_MYND_1 | 333 | 337 | PF01753 | 0.646 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.593 |
LIG_SH2_GRB2like | 374 | 377 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.601 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.563 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.702 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.703 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.363 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.809 |
LIG_SUMO_SIM_anti_2 | 132 | 138 | PF11976 | 0.539 |
LIG_SUMO_SIM_anti_2 | 377 | 384 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 381 | 386 | PF11976 | 0.465 |
LIG_TYR_ITIM | 52 | 57 | PF00017 | 0.628 |
LIG_WRC_WIRS_1 | 36 | 41 | PF05994 | 0.575 |
MOD_CDK_SPK_2 | 86 | 91 | PF00069 | 0.583 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.672 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.738 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.608 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.569 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.635 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.744 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.683 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.803 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.572 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.619 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.812 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.533 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.717 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.476 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.674 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.706 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.591 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.767 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.772 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.711 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.665 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.797 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.353 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.358 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.745 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.659 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.587 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.599 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.761 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.688 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.760 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.819 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.787 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.689 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.406 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.424 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.298 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.564 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.612 |
MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.782 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.748 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.343 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.816 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.645 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.762 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.632 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.810 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.552 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.726 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.607 |
MOD_PKB_1 | 184 | 192 | PF00069 | 0.577 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.578 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.557 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.495 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.602 |
MOD_Plk_2-3 | 378 | 384 | PF00069 | 0.468 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.674 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.504 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.441 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.703 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.651 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.824 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.649 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.787 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.453 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.513 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.616 |
MOD_SUMO_rev_2 | 445 | 454 | PF00179 | 0.725 |
TRG_DiLeu_BaEn_1 | 378 | 383 | PF01217 | 0.565 |
TRG_DiLeu_BaEn_2 | 34 | 40 | PF01217 | 0.573 |
TRG_DiLeu_BaEn_3 | 410 | 416 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.609 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.556 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.781 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IB32 | Leishmania donovani | 69% | 100% |
A4HZP2 | Leishmania infantum | 69% | 100% |
C9ZSD2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AVJ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
Q4QBY1 | Leishmania major | 69% | 100% |