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: Q9NE60
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.601 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.595 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.679 |
DEG_APCC_DBOX_1 | 80 | 88 | PF00400 | 0.518 |
DOC_CKS1_1 | 304 | 309 | PF01111 | 0.614 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.709 |
DOC_MAPK_MEF2A_6 | 81 | 90 | PF00069 | 0.425 |
DOC_PP1_RVXF_1 | 125 | 131 | PF00149 | 0.378 |
DOC_PP2B_PxIxI_1 | 454 | 460 | PF00149 | 0.600 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.552 |
DOC_PP4_FxxP_1 | 347 | 350 | PF00568 | 0.599 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.474 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.557 |
DOC_USP7_UBL2_3 | 33 | 37 | PF12436 | 0.558 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.813 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.397 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 195 | 204 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 364 | 370 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 469 | 478 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.591 |
LIG_Actin_WH2_2 | 519 | 535 | PF00022 | 0.563 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.723 |
LIG_BRCT_BRCA1_1 | 374 | 378 | PF00533 | 0.478 |
LIG_BRCT_BRCA1_1 | 519 | 523 | PF00533 | 0.582 |
LIG_deltaCOP1_diTrp_1 | 229 | 237 | PF00928 | 0.526 |
LIG_deltaCOP1_diTrp_1 | 59 | 67 | PF00928 | 0.577 |
LIG_EH1_1 | 447 | 455 | PF00400 | 0.639 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.598 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.613 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.618 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.602 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.492 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.515 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.429 |
LIG_GBD_Chelix_1 | 125 | 133 | PF00786 | 0.373 |
LIG_LIR_Apic_2 | 102 | 106 | PF02991 | 0.480 |
LIG_LIR_Apic_2 | 236 | 240 | PF02991 | 0.618 |
LIG_LIR_Apic_2 | 306 | 311 | PF02991 | 0.707 |
LIG_LIR_Apic_2 | 345 | 350 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 115 | 122 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 520 | 526 | PF02991 | 0.583 |
LIG_MYND_1 | 307 | 311 | PF01753 | 0.610 |
LIG_NRBOX | 16 | 22 | PF00104 | 0.361 |
LIG_NRBOX | 502 | 508 | PF00104 | 0.514 |
LIG_PTAP_UEV_1 | 518 | 523 | PF05743 | 0.581 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.403 |
LIG_SH2_GRB2like | 89 | 92 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 55 | 59 | PF00017 | 0.487 |
LIG_SH2_SRC | 89 | 92 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 391 | 395 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.710 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.402 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.658 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.600 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.473 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.324 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.738 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.632 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.609 |
LIG_SUMO_SIM_par_1 | 313 | 319 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 93 | 99 | PF11976 | 0.383 |
LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.550 |
LIG_TRFH_1 | 347 | 351 | PF08558 | 0.603 |
LIG_UBA3_1 | 506 | 514 | PF00899 | 0.534 |
LIG_WW_3 | 172 | 176 | PF00397 | 0.635 |
MOD_CDC14_SPxK_1 | 268 | 271 | PF00782 | 0.664 |
MOD_CDK_SPK_2 | 321 | 326 | PF00069 | 0.663 |
MOD_CDK_SPxK_1 | 265 | 271 | PF00069 | 0.671 |
MOD_CDK_SPxxK_3 | 26 | 33 | PF00069 | 0.461 |
MOD_CDK_SPxxK_3 | 271 | 278 | PF00069 | 0.654 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.517 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.626 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.728 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.616 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.530 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.728 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.723 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.610 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.701 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.622 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.578 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.392 |
MOD_Cter_Amidation | 435 | 438 | PF01082 | 0.724 |
MOD_DYRK1A_RPxSP_1 | 181 | 185 | PF00069 | 0.552 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.554 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.692 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.671 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.682 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.482 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.582 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.569 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.623 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.501 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.529 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.658 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.570 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.623 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.617 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.681 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.641 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.656 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.538 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.749 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.392 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.691 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.630 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.683 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.511 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.561 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.700 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.618 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.690 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.714 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.449 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.682 |
MOD_NEK2_2 | 45 | 50 | PF00069 | 0.542 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.704 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.691 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.664 |
MOD_PK_1 | 287 | 293 | PF00069 | 0.676 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.644 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.621 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.658 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.454 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.489 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.496 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.647 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.445 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.606 |
MOD_Plk_2-3 | 51 | 57 | PF00069 | 0.475 |
MOD_Plk_2-3 | 96 | 102 | PF00069 | 0.399 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.389 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.640 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.634 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.574 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.595 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.555 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.666 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.597 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.613 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.731 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.570 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.727 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.623 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.652 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.624 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.570 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.523 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.609 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.652 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.392 |
TRG_DiLeu_BaEn_1 | 449 | 454 | PF01217 | 0.641 |
TRG_DiLeu_BaLyEn_6 | 12 | 17 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.381 |
TRG_DiLeu_BaLyEn_6 | 467 | 472 | PF01217 | 0.598 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.511 |
TRG_NLS_Bipartite_1 | 423 | 441 | PF00514 | 0.723 |
TRG_NLS_MonoCore_2 | 436 | 441 | PF00514 | 0.549 |
TRG_Pf-PMV_PEXEL_1 | 470 | 475 | PF00026 | 0.654 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9W6 | Leptomonas seymouri | 48% | 98% |
A0A3S7X3G8 | Leishmania donovani | 96% | 100% |
A4HIE3 | Leishmania braziliensis | 78% | 100% |
A4I5P0 | Leishmania infantum | 96% | 100% |
E9B0Y4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |