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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B4T2
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 6 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 6 |
GO:0042254 | ribosome biogenesis | 5 | 6 |
GO:0044085 | cellular component biogenesis | 3 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.713 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.792 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.732 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.717 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.753 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.377 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.699 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 227 | 236 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 12 | 19 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 154 | 160 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 24 | 31 | PF00069 | 0.577 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.712 |
DOC_USP7_UBL2_3 | 24 | 28 | PF12436 | 0.556 |
DOC_USP7_UBL2_3 | 420 | 424 | PF12436 | 0.615 |
DOC_USP7_UBL2_3 | 464 | 468 | PF12436 | 0.768 |
DOC_USP7_UBL2_3 | 501 | 505 | PF12436 | 0.707 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.677 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.600 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.581 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.565 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.629 |
LIG_LIR_Gen_1 | 56 | 67 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.577 |
LIG_NRBOX | 159 | 165 | PF00104 | 0.577 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.577 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.584 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 113 | 119 | PF11976 | 0.577 |
LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.447 |
LIG_SUMO_SIM_anti_2 | 223 | 229 | PF11976 | 0.370 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.641 |
LIG_TRAF2_1 | 492 | 495 | PF00917 | 0.728 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.582 |
LIG_UBA3_1 | 232 | 241 | PF00899 | 0.556 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.464 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.765 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.620 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.577 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.577 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.564 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.776 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.577 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.709 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.595 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.514 |
MOD_Cter_Amidation | 420 | 423 | PF01082 | 0.782 |
MOD_Cter_Amidation | 441 | 444 | PF01082 | 0.729 |
MOD_Cter_Amidation | 462 | 465 | PF01082 | 0.758 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.691 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.609 |
MOD_GlcNHglycan | 268 | 272 | PF01048 | 0.453 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.729 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.527 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.627 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.611 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.381 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.784 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.633 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.540 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.778 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.554 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.607 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.527 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.539 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.777 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.708 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.782 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.587 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.397 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.458 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.514 |
MOD_PIKK_1 | 351 | 357 | PF00454 | 0.559 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.776 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.636 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.596 |
MOD_PKA_1 | 424 | 430 | PF00069 | 0.563 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.630 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.543 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.534 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.645 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.545 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.470 |
MOD_Plk_2-3 | 487 | 493 | PF00069 | 0.532 |
MOD_Plk_2-3 | 79 | 85 | PF00069 | 0.431 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.446 |
MOD_SUMO_for_1 | 240 | 243 | PF00179 | 0.424 |
MOD_SUMO_for_1 | 27 | 30 | PF00179 | 0.556 |
MOD_SUMO_for_1 | 481 | 484 | PF00179 | 0.540 |
MOD_SUMO_rev_2 | 69 | 76 | PF00179 | 0.420 |
TRG_NES_CRM1_1 | 138 | 150 | PF08389 | 0.577 |
TRG_NES_CRM1_1 | 389 | 400 | PF08389 | 0.723 |
TRG_NLS_MonoCore_2 | 421 | 426 | PF00514 | 0.720 |
TRG_NLS_MonoExtC_3 | 463 | 468 | PF00514 | 0.766 |
TRG_NLS_MonoExtN_4 | 420 | 427 | PF00514 | 0.779 |
TRG_NLS_MonoExtN_4 | 462 | 468 | PF00514 | 0.769 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IFC9 | Leishmania donovani | 88% | 100% |
A4HAM9 | Leishmania braziliensis | 72% | 99% |
A4I9S1 | Leishmania infantum | 88% | 100% |
Q4Q394 | Leishmania major | 86% | 100% |