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: A4HAM9
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 7 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 7 |
GO:0042254 | ribosome biogenesis | 5 | 7 |
GO:0044085 | cellular component biogenesis | 3 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.493 |
CLV_C14_Caspase3-7 | 363 | 367 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 481 | 485 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.753 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.589 |
CLV_PCSK_FUR_1 | 352 | 356 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.832 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.300 |
DEG_SCF_TRCP1_1 | 366 | 372 | PF00400 | 0.545 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 227 | 236 | PF00134 | 0.518 |
DOC_MAPK_gen_1 | 12 | 19 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 154 | 160 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 24 | 31 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 310 | 317 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 374 | 383 | PF00069 | 0.533 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.663 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 415 | 419 | PF12436 | 0.605 |
DOC_USP7_UBL2_3 | 457 | 461 | PF12436 | 0.756 |
DOC_USP7_UBL2_3 | 464 | 468 | PF12436 | 0.665 |
DOC_USP7_UBL2_3 | 494 | 498 | PF12436 | 0.624 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 292 | 301 | PF00244 | 0.552 |
LIG_Actin_WH2_2 | 128 | 143 | PF00022 | 0.418 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.664 |
LIG_BRCT_BRCA1_1 | 394 | 398 | PF00533 | 0.550 |
LIG_deltaCOP1_diTrp_1 | 511 | 517 | PF00928 | 0.717 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.584 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.376 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.547 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.574 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.573 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.559 |
LIG_FHA_2 | 479 | 485 | PF00498 | 0.543 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.560 |
LIG_LIR_Gen_1 | 56 | 67 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.486 |
LIG_NRBOX | 159 | 165 | PF00104 | 0.560 |
LIG_NRBOX | 262 | 268 | PF00104 | 0.472 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.560 |
LIG_SUMO_SIM_anti_2 | 113 | 119 | PF11976 | 0.486 |
LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 223 | 229 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 311 | 317 | PF11976 | 0.532 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.702 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.487 |
LIG_UBA3_1 | 232 | 241 | PF00899 | 0.431 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.493 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.553 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.676 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.560 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.556 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.557 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.757 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.587 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.665 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.599 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.487 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.486 |
MOD_Cter_Amidation | 337 | 340 | PF01082 | 0.697 |
MOD_Cter_Amidation | 352 | 355 | PF01082 | 0.541 |
MOD_Cter_Amidation | 413 | 416 | PF01082 | 0.680 |
MOD_Cter_Amidation | 465 | 468 | PF01082 | 0.650 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.680 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.644 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.593 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.621 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.694 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.629 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.600 |
MOD_GlcNHglycan | 370 | 374 | PF01048 | 0.607 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.375 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.766 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.558 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.601 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.386 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.677 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.623 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.591 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.545 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.579 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.725 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.767 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.482 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.632 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.483 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.491 |
MOD_PIKK_1 | 428 | 434 | PF00454 | 0.748 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.519 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.487 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.559 |
MOD_PKA_1 | 456 | 462 | PF00069 | 0.551 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.497 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.526 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.486 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.553 |
MOD_PKB_1 | 454 | 462 | PF00069 | 0.551 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.555 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.552 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.469 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.375 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.532 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.479 |
MOD_SUMO_for_1 | 240 | 243 | PF00179 | 0.392 |
MOD_SUMO_for_1 | 27 | 30 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 262 | 272 | PF00179 | 0.465 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.570 |
TRG_NES_CRM1_1 | 138 | 150 | PF08389 | 0.486 |
TRG_NES_CRM1_1 | 382 | 393 | PF08389 | 0.614 |
TRG_NLS_Bipartite_1 | 437 | 459 | PF00514 | 0.540 |
TRG_NLS_MonoCore_2 | 454 | 459 | PF00514 | 0.552 |
TRG_NLS_MonoExtC_3 | 414 | 419 | PF00514 | 0.568 |
TRG_NLS_MonoExtC_3 | 455 | 460 | PF00514 | 0.746 |
TRG_NLS_MonoExtC_3 | 463 | 468 | PF00514 | 0.662 |
TRG_NLS_MonoExtN_4 | 413 | 419 | PF00514 | 0.669 |
TRG_NLS_MonoExtN_4 | 454 | 461 | PF00514 | 0.746 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IFC9 | Leishmania donovani | 71% | 99% |
A0A422NGQ3 | Trypanosoma rangeli | 51% | 100% |
A4I9S1 | Leishmania infantum | 72% | 99% |
E9B4T2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 99% |
Q4Q394 | Leishmania major | 73% | 100% |