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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AD99
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003743 | translation initiation factor activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.218 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.444 |
CLV_PCSK_FUR_1 | 235 | 239 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 341 | 343 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.587 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.468 |
DEG_COP1_1 | 206 | 215 | PF00400 | 0.496 |
DEG_COP1_1 | 423 | 432 | PF00400 | 0.476 |
DEG_SPOP_SBC_1 | 502 | 506 | PF00917 | 0.504 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.563 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.402 |
DOC_MAPK_gen_1 | 339 | 346 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 413 | 422 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 8 | 18 | PF00069 | 0.584 |
DOC_MAPK_MEF2A_6 | 173 | 181 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 413 | 422 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 427 | 434 | PF00069 | 0.418 |
DOC_MIT_MIM_1 | 249 | 259 | PF04212 | 0.438 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.455 |
DOC_PP2B_LxvP_1 | 471 | 474 | PF13499 | 0.509 |
DOC_PP4_FxxP_1 | 415 | 418 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.745 |
DOC_USP7_UBL2_3 | 295 | 299 | PF12436 | 0.458 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.418 |
DOC_USP7_UBL2_3 | 45 | 49 | PF12436 | 0.477 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.557 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.665 |
LIG_14-3-3_CanoR_1 | 138 | 145 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 205 | 210 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 321 | 325 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.690 |
LIG_Actin_WH2_2 | 279 | 297 | PF00022 | 0.389 |
LIG_Actin_WH2_2 | 66 | 82 | PF00022 | 0.334 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.592 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.420 |
LIG_EVH1_1 | 465 | 469 | PF00568 | 0.369 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.372 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.429 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.441 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.422 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.468 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.425 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.633 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.584 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 479 | 485 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 220 | 231 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 518 | 527 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 326 | 330 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.432 |
LIG_MYND_1 | 469 | 473 | PF01753 | 0.455 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.418 |
LIG_SH2_CRK | 426 | 430 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 327 | 330 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.418 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.526 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.488 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.369 |
LIG_SUMO_SIM_anti_2 | 176 | 182 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 109 | 115 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 206 | 214 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 342 | 348 | PF11976 | 0.418 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.528 |
LIG_TRAF2_1 | 4 | 7 | PF00917 | 0.491 |
LIG_TRFH_1 | 512 | 516 | PF08558 | 0.418 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.512 |
LIG_TYR_ITIM | 368 | 373 | PF00017 | 0.418 |
LIG_UBA3_1 | 286 | 295 | PF00899 | 0.381 |
MOD_CDK_SPxK_1 | 481 | 487 | PF00069 | 0.507 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.438 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.339 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.446 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.480 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.486 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.654 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.540 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.570 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.629 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.407 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.514 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.470 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.309 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.418 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.520 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.574 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.634 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.489 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.388 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.351 |
MOD_GlcNHglycan | 239 | 243 | PF01048 | 0.368 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.550 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.267 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.204 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.312 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.288 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.277 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.219 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.419 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.323 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.656 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.635 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.385 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.440 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.454 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.551 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.460 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.604 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.512 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.570 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.256 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.293 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.349 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.433 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.487 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.433 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.549 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.355 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.493 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.466 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.557 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.447 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.423 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.503 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.560 |
MOD_PKB_1 | 236 | 244 | PF00069 | 0.325 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.458 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.375 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.430 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.411 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.527 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.419 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.327 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.485 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.440 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.418 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.464 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.731 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.436 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.422 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.485 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.413 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.666 |
MOD_SUMO_rev_2 | 2 | 10 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 288 | 297 | PF00179 | 0.445 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.402 |
TRG_DiLeu_BaEn_1 | 182 | 187 | PF01217 | 0.431 |
TRG_DiLeu_BaEn_2 | 423 | 429 | PF01217 | 0.418 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.239 |
TRG_NLS_Bipartite_1 | 37 | 52 | PF00514 | 0.457 |
TRG_NLS_MonoExtN_4 | 45 | 52 | PF00514 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1D4 | Leptomonas seymouri | 70% | 82% |
A0A1X0P4F2 | Trypanosomatidae | 45% | 95% |
A0A3Q8IE91 | Leishmania donovani | 93% | 83% |
A0A422MX80 | Trypanosoma rangeli | 53% | 91% |
A4HFP5 | Leishmania braziliensis | 89% | 100% |
A4I2S1 | Leishmania infantum | 93% | 83% |
D0A5X8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 89% |
E9AZ24 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
P41111 | Oryctolagus cuniculus | 27% | 100% |
Q09924 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
Q3T058 | Bos taurus | 26% | 100% |
Q54FM3 | Dictyostelium discoideum | 25% | 90% |
Q61749 | Mus musculus | 25% | 100% |
Q63186 | Rattus norvegicus | 25% | 100% |
Q9UI10 | Homo sapiens | 25% | 100% |
V5BHQ4 | Trypanosoma cruzi | 53% | 100% |