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: 3, no: 5 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4QGG3
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.756 |
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.491 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.731 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.773 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.715 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 388 | 390 | PF00082 | 0.435 |
CLV_PCSK_PC7_1 | 152 | 158 | PF00082 | 0.624 |
CLV_PCSK_PC7_1 | 411 | 417 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.602 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.682 |
DEG_SPOP_SBC_1 | 139 | 143 | PF00917 | 0.560 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.600 |
DOC_ANK_TNKS_1 | 271 | 278 | PF00023 | 0.378 |
DOC_CYCLIN_yCln2_LP_2 | 391 | 397 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 326 | 335 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 388 | 395 | PF00069 | 0.501 |
DOC_MAPK_JIP1_4 | 389 | 395 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 20 | 29 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 388 | 395 | PF00069 | 0.517 |
DOC_PP2B_LxvP_1 | 391 | 394 | PF13499 | 0.464 |
DOC_PP2B_PxIxI_1 | 305 | 311 | PF00149 | 0.357 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.647 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.550 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.681 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.692 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.576 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.418 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.459 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.596 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.617 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.572 |
LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 216 | 225 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 62 | 70 | PF02991 | 0.498 |
LIG_LIR_LC3C_4 | 396 | 400 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.645 |
LIG_Pex14_1 | 374 | 378 | PF04695 | 0.340 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.317 |
LIG_SH2_SRC | 366 | 369 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 368 | 371 | PF00017 | 0.352 |
LIG_SH2_STAT3 | 378 | 381 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.377 |
LIG_SH3_1 | 10 | 16 | PF00018 | 0.626 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.626 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.425 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.491 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.749 |
LIG_SUMO_SIM_par_1 | 27 | 34 | PF11976 | 0.557 |
LIG_SUMO_SIM_par_1 | 396 | 403 | PF11976 | 0.473 |
LIG_TRAF2_1 | 70 | 73 | PF00917 | 0.497 |
LIG_WRC_WIRS_1 | 60 | 65 | PF05994 | 0.506 |
MOD_CDK_SPK_2 | 240 | 245 | PF00069 | 0.454 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.690 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.560 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.481 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.392 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.617 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.648 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.477 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.595 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.419 |
MOD_Cter_Amidation | 259 | 262 | PF01082 | 0.455 |
MOD_Cter_Amidation | 386 | 389 | PF01082 | 0.414 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.630 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.581 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.600 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.622 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.477 |
MOD_GlcNHglycan | 53 | 57 | PF01048 | 0.588 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.779 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.641 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.559 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.464 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.644 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.483 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.539 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.397 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.564 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.540 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.647 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.552 |
MOD_LATS_1 | 113 | 119 | PF00433 | 0.675 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.659 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.602 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.502 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.404 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.533 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.310 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.527 |
MOD_NEK2_2 | 329 | 334 | PF00069 | 0.420 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.403 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.604 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.531 |
MOD_PKA_1 | 411 | 417 | PF00069 | 0.797 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.689 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.393 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.381 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.716 |
MOD_PKA_2 | 421 | 427 | PF00069 | 0.604 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.571 |
MOD_Plk_2-3 | 354 | 360 | PF00069 | 0.441 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.535 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.401 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.358 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.479 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.397 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.457 |
TRG_DiLeu_BaEn_1 | 338 | 343 | PF01217 | 0.374 |
TRG_DiLeu_BaEn_2 | 16 | 22 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.305 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 271 | 274 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.749 |
TRG_Pf-PMV_PEXEL_1 | 213 | 218 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7W8 | Leptomonas seymouri | 55% | 96% |
A0A3R7L7Q9 | Trypanosoma rangeli | 35% | 97% |
A0A3S7WS83 | Leishmania donovani | 94% | 99% |
A4H706 | Leishmania braziliensis | 75% | 100% |
E9AGI8 | Leishmania infantum | 94% | 99% |
E9AP26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
V5DFZ8 | Trypanosoma cruzi | 34% | 98% |