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: A4HVT3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.538 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.765 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.575 |
CLV_PCSK_FUR_1 | 481 | 485 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.643 |
CLV_PCSK_PC7_1 | 47 | 53 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.521 |
DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.395 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.397 |
DEG_APCC_DBOX_1 | 385 | 393 | PF00400 | 0.614 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.628 |
DOC_CKS1_1 | 394 | 399 | PF01111 | 0.628 |
DOC_CYCLIN_yCln2_LP_2 | 175 | 181 | PF00134 | 0.590 |
DOC_PP2B_LxvP_1 | 112 | 115 | PF13499 | 0.574 |
DOC_PP2B_LxvP_1 | 175 | 178 | PF13499 | 0.608 |
DOC_PP2B_LxvP_1 | 414 | 417 | PF13499 | 0.598 |
DOC_PP2B_LxvP_1 | 467 | 470 | PF13499 | 0.607 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.620 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.670 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 117 | 127 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 237 | 245 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 51 | 55 | PF00244 | 0.550 |
LIG_14-3-3_CterR_2 | 483 | 487 | PF00244 | 0.695 |
LIG_APCC_ABBA_1 | 157 | 162 | PF00400 | 0.583 |
LIG_APCC_ABBA_1 | 204 | 209 | PF00400 | 0.575 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.588 |
LIG_Clathr_ClatBox_1 | 226 | 230 | PF01394 | 0.395 |
LIG_Clathr_ClatBox_1 | 424 | 428 | PF01394 | 0.448 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.707 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.487 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.738 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.559 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.486 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.514 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.494 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.656 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.622 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.585 |
LIG_GBD_Chelix_1 | 227 | 235 | PF00786 | 0.476 |
LIG_GBD_Chelix_1 | 303 | 311 | PF00786 | 0.404 |
LIG_KLC1_Yacidic_2 | 158 | 162 | PF13176 | 0.590 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.626 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.445 |
LIG_NRBOX | 462 | 468 | PF00104 | 0.596 |
LIG_PDZ_Class_1 | 482 | 487 | PF00595 | 0.697 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.401 |
LIG_Rb_pABgroove_1 | 148 | 156 | PF01858 | 0.578 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.452 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.600 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.579 |
LIG_SH2_GRB2like | 317 | 320 | PF00017 | 0.386 |
LIG_SH2_SRC | 160 | 163 | PF00017 | 0.593 |
LIG_SH2_SRC | 317 | 320 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.643 |
LIG_SH2_STAT3 | 338 | 341 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.469 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.581 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.533 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.350 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.810 |
LIG_SUMO_SIM_anti_2 | 421 | 430 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 103 | 110 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 224 | 230 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 421 | 430 | PF11976 | 0.520 |
LIG_WW_3 | 114 | 118 | PF00397 | 0.611 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.760 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.630 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.544 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.600 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.622 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.503 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.403 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.420 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.659 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.707 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.653 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.577 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.706 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.726 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.572 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.687 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.569 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.596 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.679 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.593 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.482 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.679 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.600 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.654 |
MOD_N-GLC_2 | 372 | 374 | PF02516 | 0.579 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.606 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.632 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.433 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.608 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.523 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.579 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.653 |
MOD_NEK2_2 | 381 | 386 | PF00069 | 0.671 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.584 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.591 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.517 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.548 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.569 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.553 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.548 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.627 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.533 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.510 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.655 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.358 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.668 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.549 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.688 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.563 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.458 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.623 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.586 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.653 |
TRG_DiLeu_BaEn_1 | 462 | 467 | PF01217 | 0.589 |
TRG_DiLeu_BaEn_2 | 18 | 24 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 84 | 89 | PF01217 | 0.585 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.578 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.636 |
TRG_NES_CRM1_1 | 148 | 162 | PF08389 | 0.532 |
TRG_NLS_Bipartite_1 | 346 | 361 | PF00514 | 0.589 |
TRG_NLS_MonoExtN_4 | 355 | 361 | PF00514 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 257 | 262 | PF00026 | 0.477 |
TRG_PTS1 | 484 | 487 | PF00515 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8K4 | Leptomonas seymouri | 48% | 83% |
A0A3S7WSN4 | Leishmania donovani | 100% | 100% |
A4H7E3 | Leishmania braziliensis | 75% | 100% |
E9APH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QG00 | Leishmania major | 92% | 100% |