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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HNR0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 433 | 437 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.771 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.630 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.675 |
DEG_ODPH_VHL_1 | 275 | 286 | PF01847 | 0.619 |
DOC_CYCLIN_yCln2_LP_2 | 285 | 288 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 198 | 205 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 332 | 338 | PF00069 | 0.602 |
DOC_PIKK_1 | 22 | 30 | PF02985 | 0.392 |
DOC_PP1_RVXF_1 | 159 | 166 | PF00149 | 0.531 |
DOC_PP2B_LxvP_1 | 285 | 288 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 349 | 352 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.769 |
DOC_PP2B_PxIxI_1 | 326 | 332 | PF00149 | 0.707 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.601 |
DOC_PP4_FxxP_1 | 266 | 269 | PF00568 | 0.485 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.639 |
LIG_14-3-3_CanoR_1 | 313 | 322 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 38 | 47 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 99 | 104 | PF00244 | 0.691 |
LIG_Actin_WH2_2 | 374 | 392 | PF00022 | 0.627 |
LIG_BRCT_BRCA1_1 | 231 | 235 | PF00533 | 0.415 |
LIG_Clathr_ClatBox_1 | 378 | 382 | PF01394 | 0.632 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.475 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.562 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.515 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.558 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.501 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.534 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.592 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.336 |
LIG_GBD_Chelix_1 | 10 | 18 | PF00786 | 0.590 |
LIG_Integrin_RGD_1 | 149 | 151 | PF01839 | 0.346 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.381 |
LIG_LIR_Apic_2 | 264 | 269 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 126 | 134 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 242 | 253 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.469 |
LIG_NRBOX | 126 | 132 | PF00104 | 0.552 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.521 |
LIG_Pex14_2 | 262 | 266 | PF04695 | 0.423 |
LIG_Rb_LxCxE_1 | 247 | 265 | PF01857 | 0.587 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.358 |
LIG_SH2_SRC | 267 | 270 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.509 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.383 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.601 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.531 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.576 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.717 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.671 |
LIG_SUMO_SIM_anti_2 | 374 | 380 | PF11976 | 0.632 |
LIG_SUMO_SIM_par_1 | 293 | 299 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 377 | 382 | PF11976 | 0.632 |
LIG_WRC_WIRS_1 | 263 | 268 | PF05994 | 0.596 |
MOD_CDK_SPK_2 | 94 | 99 | PF00069 | 0.515 |
MOD_CDK_SPxxK_3 | 55 | 62 | PF00069 | 0.669 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.604 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.298 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.573 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.503 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.332 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.558 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.538 |
MOD_Cter_Amidation | 196 | 199 | PF01082 | 0.658 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.468 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.434 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.406 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.581 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.465 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.323 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.738 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.559 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.664 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.596 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.467 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.564 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.609 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.607 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.664 |
MOD_NEK2_2 | 244 | 249 | PF00069 | 0.535 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.608 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.494 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.545 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.578 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.581 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.517 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.395 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.558 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.671 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.332 |
MOD_Plk_2-3 | 414 | 420 | PF00069 | 0.322 |
MOD_Plk_2-3 | 430 | 436 | PF00069 | 0.337 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.427 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.518 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.602 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.674 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.615 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.382 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.696 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.733 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.637 |
MOD_SUMO_for_1 | 427 | 430 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 414 | 422 | PF00179 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 133 | 138 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.573 |
TRG_NLS_MonoExtN_4 | 32 | 39 | PF00514 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JPJ4 | Bodo saltans | 31% | 86% |
A0A1X0P9M8 | Trypanosomatidae | 36% | 99% |
A0A3Q8IFS3 | Leishmania donovani | 73% | 100% |
A0A422P297 | Trypanosoma rangeli | 36% | 99% |
A4ICT5 | Leishmania infantum | 74% | 100% |
D0A2L8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 99% |
E9ASG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q226 | Leishmania major | 72% | 100% |