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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H548
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 201 | 205 | PF00656 | 0.715 |
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.851 |
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.708 |
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.666 |
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.800 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.509 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.538 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.558 |
DOC_CYCLIN_yClb3_PxF_3 | 79 | 85 | PF00134 | 0.433 |
DOC_CYCLIN_yCln2_LP_2 | 151 | 157 | PF00134 | 0.243 |
DOC_MAPK_DCC_7 | 9 | 19 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 148 | 157 | PF00069 | 0.238 |
DOC_MAPK_MEF2A_6 | 207 | 214 | PF00069 | 0.533 |
DOC_MAPK_NFAT4_5 | 207 | 215 | PF00069 | 0.533 |
DOC_PP1_RVXF_1 | 44 | 50 | PF00149 | 0.494 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.527 |
DOC_PP2B_LxvP_1 | 151 | 154 | PF13499 | 0.527 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.622 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 46 | 50 | PF00244 | 0.491 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.531 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.475 |
LIG_DLG_GKlike_1 | 13 | 21 | PF00625 | 0.514 |
LIG_EVH1_2 | 81 | 85 | PF00568 | 0.440 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.527 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.468 |
LIG_LIR_Gen_1 | 48 | 56 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 91 | 99 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 91 | 95 | PF02991 | 0.373 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.484 |
LIG_PTAP_UEV_1 | 303 | 308 | PF05743 | 0.847 |
LIG_REV1ctd_RIR_1 | 165 | 174 | PF16727 | 0.527 |
LIG_SH2_NCK_1 | 139 | 143 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.527 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.847 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.430 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.551 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.687 |
MOD_CDK_SPxxK_3 | 358 | 365 | PF00069 | 0.734 |
MOD_CDK_SPxxK_3 | 367 | 374 | PF00069 | 0.631 |
MOD_CDK_SPxxK_3 | 376 | 383 | PF00069 | 0.673 |
MOD_CDK_SPxxK_3 | 385 | 392 | PF00069 | 0.812 |
MOD_CDK_SPxxK_3 | 394 | 401 | PF00069 | 0.753 |
MOD_CDK_SPxxK_3 | 403 | 410 | PF00069 | 0.588 |
MOD_CDK_SPxxK_3 | 412 | 419 | PF00069 | 0.571 |
MOD_CDK_SPxxK_3 | 421 | 428 | PF00069 | 0.655 |
MOD_CDK_SPxxK_3 | 439 | 446 | PF00069 | 0.638 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.488 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.527 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.503 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.718 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.852 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.602 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.634 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.272 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.764 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.571 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.653 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.842 |
MOD_Cter_Amidation | 453 | 456 | PF01082 | 0.574 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.484 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.388 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.846 |
MOD_GlcNHglycan | 248 | 252 | PF01048 | 0.777 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.850 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.705 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.703 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.631 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.827 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.735 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.367 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.583 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.684 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.780 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.539 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.845 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.860 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.697 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.650 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.613 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.602 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.516 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.243 |
MOD_LATS_1 | 7 | 13 | PF00433 | 0.519 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.588 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.549 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.369 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.475 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.506 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.435 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.450 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.442 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.404 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.527 |
MOD_NEK2_2 | 171 | 176 | PF00069 | 0.369 |
MOD_NEK2_2 | 45 | 50 | PF00069 | 0.492 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.394 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.509 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.520 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.544 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.478 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.579 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.861 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.710 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.786 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.633 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.553 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.697 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.491 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.504 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.753 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.571 |
MOD_Plk_2-3 | 252 | 258 | PF00069 | 0.846 |
MOD_Plk_2-3 | 268 | 274 | PF00069 | 0.579 |
MOD_Plk_2-3 | 321 | 327 | PF00069 | 0.825 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.454 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.286 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.429 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.783 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.754 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.700 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.789 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.731 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.586 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.570 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.656 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.637 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.527 |
MOD_SUMO_rev_2 | 133 | 138 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_1 | 238 | 243 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_4 | 322 | 328 | PF01217 | 0.560 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQ00 | Leishmania donovani | 64% | 100% |
A4HTC4 | Leishmania infantum | 63% | 100% |
E9ALB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QII7 | Leishmania major | 68% | 99% |