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: A4I419
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.677 |
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.681 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.434 |
CLV_PCSK_FUR_1 | 273 | 277 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.429 |
DEG_COP1_1 | 130 | 138 | PF00400 | 0.588 |
DEG_SCF_FBW7_1 | 7 | 14 | PF00400 | 0.445 |
DEG_SPOP_SBC_1 | 227 | 231 | PF00917 | 0.520 |
DEG_SPOP_SBC_1 | 342 | 346 | PF00917 | 0.694 |
DOC_ANK_TNKS_1 | 73 | 80 | PF00023 | 0.521 |
DOC_CKS1_1 | 135 | 140 | PF01111 | 0.574 |
DOC_CKS1_1 | 251 | 256 | PF01111 | 0.440 |
DOC_CYCLIN_RxL_1 | 165 | 172 | PF00134 | 0.372 |
DOC_CYCLIN_yClb3_PxF_3 | 445 | 453 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 360 | 371 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 415 | 423 | PF00069 | 0.633 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.384 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.778 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.676 |
LIG_14-3-3_CanoR_1 | 166 | 171 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 239 | 249 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 276 | 281 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 313 | 317 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.565 |
LIG_Actin_WH2_2 | 105 | 123 | PF00022 | 0.479 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.624 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.624 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.472 |
LIG_Clathr_ClatBox_1 | 58 | 62 | PF01394 | 0.504 |
LIG_eIF4E_1 | 438 | 444 | PF01652 | 0.557 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.377 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.590 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.443 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.553 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.585 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.465 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.461 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.654 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.620 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.555 |
LIG_Integrin_RGD_1 | 364 | 366 | PF01839 | 0.677 |
LIG_LIR_Apic_2 | 435 | 441 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 467 | 475 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.341 |
LIG_MYND_1 | 441 | 445 | PF01753 | 0.553 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.353 |
LIG_NRBOX | 468 | 474 | PF00104 | 0.337 |
LIG_Pex14_2 | 5 | 9 | PF04695 | 0.472 |
LIG_Rb_pABgroove_1 | 165 | 173 | PF01858 | 0.354 |
LIG_RPA_C_Fungi | 301 | 313 | PF08784 | 0.485 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.420 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 438 | 442 | PF00017 | 0.559 |
LIG_SH2_NCK_1 | 446 | 450 | PF00017 | 0.533 |
LIG_SH2_SRC | 442 | 445 | PF00017 | 0.524 |
LIG_SH2_SRC | 446 | 449 | PF00017 | 0.502 |
LIG_SH2_STAT3 | 248 | 251 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.590 |
LIG_SH3_1 | 442 | 448 | PF00018 | 0.436 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.581 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.436 |
LIG_SUMO_SIM_anti_2 | 378 | 384 | PF11976 | 0.788 |
LIG_SUMO_SIM_anti_2 | 398 | 403 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 378 | 384 | PF11976 | 0.592 |
LIG_SUMO_SIM_par_1 | 400 | 406 | PF11976 | 0.614 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.642 |
MOD_CDK_SPK_2 | 7 | 12 | PF00069 | 0.454 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.661 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.560 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.558 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.615 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.613 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.452 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.612 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.516 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.451 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.517 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.790 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.649 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.596 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.401 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.450 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.623 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.597 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.567 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.747 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.813 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.751 |
MOD_GlcNHglycan | 391 | 395 | PF01048 | 0.670 |
MOD_GlcNHglycan | 434 | 438 | PF01048 | 0.702 |
MOD_GlcNHglycan | 465 | 469 | PF01048 | 0.442 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.612 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.528 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.650 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.530 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.629 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.823 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.630 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.708 |
MOD_LATS_1 | 303 | 309 | PF00433 | 0.481 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.486 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.618 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.471 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.621 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.415 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.525 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.458 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.406 |
MOD_PKA_1 | 175 | 181 | PF00069 | 0.429 |
MOD_PKA_1 | 305 | 311 | PF00069 | 0.489 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.458 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.572 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.432 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.562 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.511 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.537 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.731 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.613 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.628 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.655 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.335 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.448 |
MOD_Plk_2-3 | 428 | 434 | PF00069 | 0.600 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.680 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.604 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.426 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.592 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.664 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.641 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.678 |
MOD_SUMO_rev_2 | 211 | 219 | PF00179 | 0.487 |
TRG_DiLeu_BaEn_1 | 439 | 444 | PF01217 | 0.555 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.361 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.489 |
TRG_NLS_MonoExtC_3 | 359 | 364 | PF00514 | 0.611 |
TRG_NLS_MonoExtN_4 | 358 | 365 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYA9 | Leptomonas seymouri | 48% | 100% |
A0A3Q8IE22 | Leishmania donovani | 100% | 97% |
A4HGY7 | Leishmania braziliensis | 71% | 100% |
E9B0A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q7X8 | Leishmania major | 91% | 100% |