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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AZ24
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 | 220 | 222 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.218 |
CLV_PCSK_FUR_1 | 220 | 224 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.298 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.218 |
DEG_APCC_DBOX_1 | 24 | 32 | PF00400 | 0.469 |
DEG_COP1_1 | 192 | 200 | PF00400 | 0.490 |
DEG_COP1_1 | 408 | 417 | PF00400 | 0.475 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.421 |
DEG_SPOP_SBC_1 | 487 | 491 | PF00917 | 0.504 |
DEG_SPOP_SBC_1 | 79 | 83 | PF00917 | 0.644 |
DOC_CKS1_1 | 450 | 455 | PF01111 | 0.563 |
DOC_CKS1_1 | 467 | 472 | PF01111 | 0.402 |
DOC_MAPK_DCC_7 | 454 | 463 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 324 | 331 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 398 | 407 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 158 | 166 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 412 | 419 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 454 | 463 | PF00069 | 0.342 |
DOC_MIT_MIM_1 | 234 | 244 | PF04212 | 0.437 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 456 | 459 | PF13499 | 0.509 |
DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.747 |
DOC_USP7_UBL2_3 | 280 | 284 | PF12436 | 0.453 |
DOC_USP7_UBL2_3 | 398 | 402 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.730 |
LIG_14-3-3_CanoR_1 | 123 | 130 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 306 | 310 | PF00244 | 0.434 |
LIG_Actin_WH2_2 | 264 | 282 | PF00022 | 0.387 |
LIG_BRCT_BRCA1_1 | 409 | 413 | PF00533 | 0.420 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.391 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.425 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.441 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.421 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.468 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.428 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.644 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.537 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.582 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.382 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.432 |
LIG_LIR_Apic_2 | 464 | 470 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 503 | 512 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 311 | 315 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 354 | 358 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.432 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.418 |
LIG_SH2_CRK | 411 | 415 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 312 | 315 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.418 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.516 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.489 |
LIG_SUMO_SIM_anti_2 | 161 | 167 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 192 | 199 | PF11976 | 0.485 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 327 | 333 | PF11976 | 0.418 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.518 |
LIG_TRFH_1 | 497 | 501 | PF08558 | 0.418 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.512 |
LIG_TYR_ITIM | 353 | 358 | PF00017 | 0.418 |
LIG_UBA3_1 | 271 | 280 | PF00899 | 0.379 |
MOD_CDK_SPK_2 | 449 | 454 | PF00069 | 0.389 |
MOD_CDK_SPxK_1 | 466 | 472 | PF00069 | 0.507 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.437 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.337 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.446 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.497 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.480 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.583 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.541 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.630 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.402 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.509 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.467 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.307 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.418 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.531 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.529 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.493 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.389 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.349 |
MOD_GlcNHglycan | 224 | 228 | PF01048 | 0.364 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.267 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.204 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.425 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.312 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.287 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.277 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.219 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.324 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.530 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.622 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.622 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.385 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.440 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.454 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.551 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.448 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.525 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.667 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.637 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.567 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.344 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.433 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.487 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.433 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.549 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.355 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.493 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.466 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.324 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.560 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.446 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.423 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.503 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.564 |
MOD_PKB_1 | 221 | 229 | PF00069 | 0.318 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.456 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.371 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.271 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.530 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.418 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.325 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.485 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.440 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.418 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.464 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.436 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.421 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.485 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.441 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.413 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.680 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.730 |
MOD_SUMO_rev_2 | 103 | 109 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 273 | 282 | PF00179 | 0.443 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_1 | 167 | 172 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_2 | 408 | 414 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 444 | 449 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.237 |
TRG_Pf-PMV_PEXEL_1 | 340 | 344 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1D4 | Leptomonas seymouri | 71% | 80% |
A0A1X0P4F2 | Trypanosomatidae | 44% | 92% |
A0A3Q8IE91 | Leishmania donovani | 95% | 81% |
A0A422MX80 | Trypanosoma rangeli | 52% | 88% |
A4HFP5 | Leishmania braziliensis | 87% | 100% |
A4I2S1 | Leishmania infantum | 95% | 81% |
D0A5X8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 86% |
E9AD99 | Leishmania major | 93% | 100% |
P12754 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 83% |
P41111 | Oryctolagus cuniculus | 25% | 100% |
Q09924 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
Q3T058 | Bos taurus | 24% | 100% |
Q54FM3 | Dictyostelium discoideum | 24% | 87% |
Q61749 | Mus musculus | 26% | 100% |
Q63186 | Rattus norvegicus | 26% | 100% |
Q9UI10 | Homo sapiens | 25% | 100% |
V5BHQ4 | Trypanosoma cruzi | 52% | 100% |