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: 3 |
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: A0A3S7X927
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 130 | 134 | PF00656 | 0.511 |
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.478 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.612 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.612 |
CLV_PCSK_PC7_1 | 260 | 266 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.630 |
DOC_CKS1_1 | 56 | 61 | PF01111 | 0.454 |
DOC_MAPK_MEF2A_6 | 37 | 45 | PF00069 | 0.473 |
DOC_PP2B_LxvP_1 | 376 | 379 | PF13499 | 0.528 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.524 |
DOC_USP7_UBL2_3 | 252 | 256 | PF12436 | 0.659 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 152 | 160 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 168 | 175 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 320 | 324 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 361 | 370 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.438 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.461 |
LIG_BIR_III_4 | 412 | 416 | PF00653 | 0.673 |
LIG_BIR_III_4 | 438 | 442 | PF00653 | 0.624 |
LIG_Clathr_ClatBox_1 | 15 | 19 | PF01394 | 0.440 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.647 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.591 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.633 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.462 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.543 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.649 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.677 |
LIG_LIR_Gen_1 | 11 | 21 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 119 | 129 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 455 | 465 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 11 | 16 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.366 |
LIG_Pex14_2 | 359 | 363 | PF04695 | 0.551 |
LIG_SH2_PTP2 | 40 | 43 | PF00017 | 0.434 |
LIG_SH2_SRC | 40 | 43 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.358 |
LIG_SH3_1 | 267 | 273 | PF00018 | 0.704 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.704 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.582 |
LIG_TRAF2_1 | 246 | 249 | PF00917 | 0.595 |
LIG_TRAF2_2 | 245 | 250 | PF00917 | 0.674 |
LIG_UBA3_1 | 460 | 468 | PF00899 | 0.592 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.307 |
LIG_WW_3 | 377 | 381 | PF00397 | 0.616 |
MOD_CDC14_SPxK_1 | 317 | 320 | PF00782 | 0.531 |
MOD_CDK_SPxK_1 | 314 | 320 | PF00069 | 0.577 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.580 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.536 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.535 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.414 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.650 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.675 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.733 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.560 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.651 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.605 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.548 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.389 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.461 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.653 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.505 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.596 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.594 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.696 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.654 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.639 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.638 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.594 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.476 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.625 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.473 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.547 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.615 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.658 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.732 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.592 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.618 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.657 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.590 |
MOD_N-GLC_1 | 361 | 366 | PF02516 | 0.634 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.579 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.441 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.646 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.588 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.572 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.688 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.423 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.572 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.675 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.368 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.428 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.656 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.503 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.619 |
MOD_PKB_1 | 166 | 174 | PF00069 | 0.502 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.530 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.643 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.368 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.683 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.695 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.605 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.608 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.444 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P595 | Leptomonas seymouri | 39% | 95% |
A4HMI4 | Leishmania braziliensis | 49% | 88% |
A4IB64 | Leishmania infantum | 99% | 100% |
E9AEY5 | Leishmania major | 81% | 96% |
E9B641 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 91% |