Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 27 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005850 | eukaryotic translation initiation factor 2 complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H5T7
Term | Name | Level | Count |
---|---|---|---|
GO:0001731 | formation of translation preinitiation complex | 7 | 2 |
GO:0006417 | regulation of translation | 6 | 2 |
GO:0006450 | regulation of translational fidelity | 3 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0010628 | positive regulation of gene expression | 6 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 2 |
GO:0034248 | regulation of amide metabolic process | 5 | 2 |
GO:0034250 | positive regulation of amide metabolic process | 6 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0045727 | positive regulation of translation | 7 | 2 |
GO:0045903 | positive regulation of translational fidelity | 4 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003743 | translation initiation factor activity | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003924 | GTPase activity | 7 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005525 | GTP binding | 5 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019001 | guanyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion 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:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0000049 | tRNA binding | 5 | 6 |
GO:0003723 | RNA binding | 4 | 6 |
GO:0003746 | translation elongation factor activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.681 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.555 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.351 |
DOC_CDC14_PxL_1 | 301 | 309 | PF14671 | 0.442 |
DOC_CYCLIN_yCln2_LP_2 | 270 | 276 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 449 | 455 | PF00134 | 0.581 |
DOC_CYCLIN_yCln2_LP_2 | 557 | 563 | PF00134 | 0.403 |
DOC_MAPK_gen_1 | 251 | 262 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 383 | 391 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 457 | 465 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 589 | 596 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 76 | 85 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 457 | 465 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 525 | 534 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 589 | 596 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 79 | 87 | PF00069 | 0.562 |
DOC_MAPK_RevD_3 | 305 | 320 | PF00069 | 0.515 |
DOC_PP1_RVXF_1 | 579 | 586 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 449 | 452 | PF13499 | 0.584 |
DOC_PP2B_PxIxI_1 | 460 | 466 | PF00149 | 0.421 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.562 |
DOC_PP4_FxxP_1 | 361 | 364 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 255 | 263 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 346 | 350 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 513 | 518 | PF00244 | 0.403 |
LIG_Actin_WH2_2 | 240 | 257 | PF00022 | 0.530 |
LIG_Actin_WH2_2 | 462 | 479 | PF00022 | 0.424 |
LIG_Actin_WH2_2 | 510 | 527 | PF00022 | 0.286 |
LIG_Actin_WH2_2 | 530 | 547 | PF00022 | 0.351 |
LIG_APCC_ABBA_1 | 463 | 468 | PF00400 | 0.422 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.793 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.681 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.382 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.559 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.518 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.418 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.562 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.498 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.796 |
LIG_Integrin_RGD_1 | 494 | 496 | PF01839 | 0.613 |
LIG_LIR_Apic_2 | 167 | 172 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 339 | 344 | PF02991 | 0.495 |
LIG_LIR_Apic_2 | 358 | 364 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.361 |
LIG_PCNA_PIPBox_1 | 207 | 216 | PF02747 | 0.522 |
LIG_PCNA_PIPBox_1 | 467 | 476 | PF02747 | 0.458 |
LIG_PCNA_yPIPBox_3 | 460 | 474 | PF02747 | 0.453 |
LIG_REV1ctd_RIR_1 | 471 | 481 | PF16727 | 0.425 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.565 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.644 |
LIG_SH2_GRB2like | 259 | 262 | PF00017 | 0.461 |
LIG_SH2_GRB2like | 91 | 94 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.556 |
LIG_SH2_SRC | 259 | 262 | PF00017 | 0.345 |
LIG_SH2_SRC | 466 | 469 | PF00017 | 0.403 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.403 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.562 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.562 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.439 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.460 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.583 |
LIG_Sin3_3 | 158 | 165 | PF02671 | 0.562 |
LIG_SUMO_SIM_anti_2 | 187 | 193 | PF11976 | 0.518 |
LIG_SUMO_SIM_anti_2 | 299 | 305 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 366 | 373 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 528 | 536 | PF11976 | 0.391 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.461 |
LIG_TYR_ITSM | 255 | 262 | PF00017 | 0.375 |
LIG_UBA3_1 | 189 | 195 | PF00899 | 0.556 |
LIG_WRC_WIRS_1 | 263 | 268 | PF05994 | 0.489 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.519 |
MOD_CDK_SPK_2 | 403 | 408 | PF00069 | 0.606 |
MOD_CDK_SPxK_1 | 488 | 494 | PF00069 | 0.618 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.644 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.649 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.598 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.587 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.594 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.403 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.618 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.550 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.525 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.681 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.645 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.403 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.362 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.559 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.476 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.416 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.670 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.475 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.682 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.609 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.440 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.390 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.562 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.481 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.356 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.589 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.591 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.362 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.562 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.477 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.456 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.453 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.581 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.403 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.562 |
MOD_NEK2_2 | 584 | 589 | PF00069 | 0.461 |
MOD_OFUCOSY | 102 | 107 | PF10250 | 0.481 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.562 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.382 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.562 |
MOD_PK_1 | 513 | 519 | PF00069 | 0.286 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.681 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.522 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.521 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.490 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.627 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.286 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.403 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.681 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.556 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.475 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.795 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.562 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.562 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.519 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.473 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.624 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.376 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.468 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.562 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.589 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.622 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.686 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.634 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.618 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.656 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 519 | 521 | PF00400 | 0.403 |
TRG_NES_CRM1_1 | 182 | 193 | PF08389 | 0.681 |
TRG_Pf-PMV_PEXEL_1 | 595 | 599 | PF00026 | 0.570 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NJL3 | Trypanosomatidae | 55% | 100% |
A0A3S7WQT0 | Leishmania donovani | 69% | 100% |
A4H5T6 | Leishmania braziliensis | 70% | 100% |
A4HU29 | Leishmania infantum | 69% | 100% |
A4HU30 | Leishmania infantum | 85% | 100% |
E9AMV9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
E9AMW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QHR6 | Leishmania major | 86% | 100% |
Q4QHR7 | Leishmania major | 69% | 100% |