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: A4HLW9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.525 |
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.595 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.747 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.747 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.718 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.617 |
DEG_APCC_DBOX_1 | 450 | 458 | PF00400 | 0.696 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.663 |
DEG_SPOP_SBC_1 | 184 | 188 | PF00917 | 0.620 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.590 |
DEG_SPOP_SBC_1 | 384 | 388 | PF00917 | 0.486 |
DOC_ANK_TNKS_1 | 89 | 96 | PF00023 | 0.502 |
DOC_CDC14_PxL_1 | 491 | 499 | PF14671 | 0.531 |
DOC_CKS1_1 | 286 | 291 | PF01111 | 0.520 |
DOC_PP2B_LxvP_1 | 489 | 492 | PF13499 | 0.530 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 2 | 9 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 243 | 248 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 364 | 369 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 561 | 569 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 70 | 77 | PF00244 | 0.595 |
LIG_Actin_WH2_2 | 349 | 366 | PF00022 | 0.493 |
LIG_BIR_III_4 | 203 | 207 | PF00653 | 0.634 |
LIG_BIR_III_4 | 396 | 400 | PF00653 | 0.731 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.770 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.747 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.709 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.692 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.497 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.556 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.485 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.774 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.502 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.434 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.525 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.525 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.658 |
LIG_LIR_Gen_1 | 342 | 352 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.509 |
LIG_MYND_1 | 269 | 273 | PF01753 | 0.512 |
LIG_NBox_RRM_1 | 213 | 223 | PF00076 | 0.465 |
LIG_PDZ_Class_2 | 566 | 571 | PF00595 | 0.465 |
LIG_PTAP_UEV_1 | 491 | 496 | PF05743 | 0.529 |
LIG_RPA_C_Fungi | 154 | 166 | PF08784 | 0.664 |
LIG_SH2_CRK | 536 | 540 | PF00017 | 0.446 |
LIG_SH2_PTP2 | 435 | 438 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 359 | 363 | PF00017 | 0.712 |
LIG_SH2_STAP1 | 485 | 489 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 536 | 540 | PF00017 | 0.511 |
LIG_SH2_STAT3 | 39 | 42 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.524 |
LIG_SH3_2 | 269 | 274 | PF14604 | 0.519 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.719 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.551 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.576 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.681 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.597 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.529 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.731 |
LIG_SUMO_SIM_par_1 | 326 | 335 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 441 | 448 | PF11976 | 0.621 |
LIG_SUMO_SIM_par_1 | 486 | 493 | PF11976 | 0.526 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.774 |
LIG_TRFH_1 | 435 | 439 | PF08558 | 0.494 |
LIG_TYR_ITIM | 433 | 438 | PF00017 | 0.333 |
LIG_UBA3_1 | 530 | 534 | PF00899 | 0.655 |
LIG_WW_3 | 271 | 275 | PF00397 | 0.524 |
MOD_CDK_SPK_2 | 475 | 480 | PF00069 | 0.483 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.772 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.720 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.468 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.590 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.564 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.536 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.751 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.737 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.532 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.687 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.645 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.649 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.713 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.501 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.714 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.698 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.678 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.661 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.550 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.618 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.564 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.664 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.654 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.656 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.683 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.694 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.689 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.579 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.665 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.707 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.717 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.511 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.555 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.507 |
MOD_N-GLC_1 | 58 | 63 | PF02516 | 0.504 |
MOD_N-GLC_2 | 544 | 546 | PF02516 | 0.626 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.661 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.695 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.512 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.484 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.478 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.623 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.660 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.667 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.514 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.453 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.661 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.538 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.511 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.592 |
MOD_Plk_2-3 | 481 | 487 | PF00069 | 0.528 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.676 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.503 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.654 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.704 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.521 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.582 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.668 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.745 |
TRG_ER_diArg_1 | 558 | 561 | PF00400 | 0.654 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBA9 | Leptomonas seymouri | 31% | 96% |
A0A3Q8IF25 | Leishmania donovani | 63% | 99% |
A4I998 | Leishmania infantum | 64% | 99% |
E9B498 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
Q4Q3S8 | Leishmania major | 63% | 100% |