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: A4H8P3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.559 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.636 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.711 |
CLV_PCSK_PC7_1 | 152 | 158 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.510 |
CLV_Separin_Metazoa | 21 | 25 | PF03568 | 0.571 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.640 |
DEG_APCC_DBOX_1 | 245 | 253 | PF00400 | 0.486 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.504 |
DEG_SPOP_SBC_1 | 385 | 389 | PF00917 | 0.441 |
DOC_CDC14_PxL_1 | 299 | 307 | PF14671 | 0.530 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 231 | 239 | PF00134 | 0.647 |
DOC_CYCLIN_yCln2_LP_2 | 211 | 217 | PF00134 | 0.535 |
DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 202 | 211 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 392 | 399 | PF00069 | 0.599 |
DOC_MAPK_NFAT4_5 | 392 | 400 | PF00069 | 0.601 |
DOC_MAPK_RevD_3 | 400 | 414 | PF00069 | 0.445 |
DOC_PP2B_LxvP_1 | 209 | 212 | PF13499 | 0.682 |
DOC_PP2B_LxvP_1 | 247 | 250 | PF13499 | 0.447 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.637 |
DOC_PP4_FxxP_1 | 94 | 97 | PF00568 | 0.682 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.620 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 202 | 209 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 297 | 305 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 320 | 329 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 350 | 355 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 367 | 373 | PF00244 | 0.723 |
LIG_APCC_ABBA_1 | 23 | 28 | PF00400 | 0.591 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.632 |
LIG_BIR_III_4 | 136 | 140 | PF00653 | 0.564 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.521 |
LIG_CtBP_PxDLS_1 | 375 | 379 | PF00389 | 0.482 |
LIG_eIF4E_1 | 112 | 118 | PF01652 | 0.524 |
LIG_EVH1_2 | 178 | 182 | PF00568 | 0.663 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.548 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.676 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.634 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.676 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.486 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.593 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.641 |
LIG_LIR_Apic_2 | 91 | 97 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.528 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.525 |
LIG_PCNA_yPIPBox_3 | 19 | 27 | PF02747 | 0.592 |
LIG_PTAP_UEV_1 | 8 | 13 | PF05743 | 0.529 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.620 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.683 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.583 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.643 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.700 |
LIG_TYR_ITIM | 218 | 223 | PF00017 | 0.660 |
LIG_UBA3_1 | 248 | 257 | PF00899 | 0.614 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.571 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.448 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.648 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.498 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.539 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.623 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.515 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.688 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.511 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.697 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.584 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.584 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.662 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.724 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.714 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.518 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.658 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.534 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.530 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.654 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.517 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.701 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.668 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.473 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.565 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.527 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.644 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.612 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.482 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.457 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.630 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.473 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.661 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.515 |
MOD_NEK2_2 | 325 | 330 | PF00069 | 0.521 |
MOD_NEK2_2 | 83 | 88 | PF00069 | 0.521 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.667 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.632 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.542 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.554 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.749 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.584 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.543 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.723 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.447 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.584 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.648 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.651 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.500 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.671 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.493 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.493 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.513 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.687 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 231 | 236 | PF01217 | 0.660 |
TRG_DiLeu_BaLyEn_6 | 243 | 248 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.666 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.456 |
TRG_NLS_Bipartite_1 | 413 | 435 | PF00514 | 0.533 |
TRG_NLS_MonoCore_2 | 318 | 323 | PF00514 | 0.614 |
TRG_NLS_MonoCore_2 | 430 | 435 | PF00514 | 0.711 |
TRG_NLS_MonoExtC_3 | 430 | 436 | PF00514 | 0.710 |
TRG_NLS_MonoExtN_4 | 428 | 435 | PF00514 | 0.713 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q0 | Leptomonas seymouri | 30% | 100% |
A0A3Q8IAM2 | Leishmania donovani | 72% | 99% |
A4HX13 | Leishmania infantum | 72% | 99% |
E9AQS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 98% |
Q4QEQ1 | Leishmania major | 73% | 100% |