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: Q4Q3U6
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 11 |
GO:0006448 | regulation of translational elongation | 7 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009889 | regulation of biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010468 | regulation of gene expression | 5 | 11 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 11 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 11 |
GO:0017182 | peptidyl-diphthamide metabolic process | 7 | 11 |
GO:0017183 | peptidyl-diphthamide biosynthetic process from peptidyl-histidine | 4 | 11 |
GO:0018193 | peptidyl-amino acid modification | 5 | 11 |
GO:0018202 | peptidyl-histidine modification | 6 | 11 |
GO:0019222 | regulation of metabolic process | 3 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0031323 | regulation of cellular metabolic process | 4 | 11 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 11 |
GO:0034248 | regulation of amide metabolic process | 5 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 11 |
GO:0051246 | regulation of protein metabolic process | 5 | 11 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0080090 | regulation of primary metabolic process | 4 | 11 |
GO:1900247 | regulation of cytoplasmic translational elongation | 8 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 11 |
GO:0090560 | 2-(3-amino-3-carboxypropyl)histidine synthase activity | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.534 |
CLV_MEL_PAP_1 | 627 | 633 | PF00089 | 0.677 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.336 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 467 | 469 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 508 | 510 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.563 |
CLV_PCSK_PC7_1 | 463 | 469 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.601 |
DEG_Kelch_Keap1_1 | 269 | 274 | PF01344 | 0.633 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.366 |
DEG_SPOP_SBC_1 | 267 | 271 | PF00917 | 0.626 |
DEG_SPOP_SBC_1 | 287 | 291 | PF00917 | 0.671 |
DEG_SPOP_SBC_1 | 543 | 547 | PF00917 | 0.320 |
DOC_MAPK_gen_1 | 467 | 474 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 434 | 443 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.232 |
DOC_MAPK_NFAT4_5 | 87 | 95 | PF00069 | 0.232 |
DOC_PP2B_PxIxI_1 | 205 | 211 | PF00149 | 0.411 |
DOC_PP4_FxxP_1 | 512 | 515 | PF00568 | 0.496 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.629 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 226 | 236 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 245 | 250 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 286 | 296 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 434 | 443 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 587 | 595 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 76 | 81 | PF00244 | 0.666 |
LIG_BIR_III_2 | 574 | 578 | PF00653 | 0.529 |
LIG_BIR_III_4 | 155 | 159 | PF00653 | 0.376 |
LIG_deltaCOP1_diTrp_1 | 274 | 284 | PF00928 | 0.492 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.612 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.415 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.473 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.491 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.583 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.539 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.670 |
LIG_GBD_Chelix_1 | 175 | 183 | PF00786 | 0.420 |
LIG_LIR_Apic_2 | 510 | 515 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 299 | 309 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 321 | 331 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 490 | 499 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 545 | 555 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 449 | 454 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 469 | 473 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 490 | 495 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 621 | 627 | PF02991 | 0.541 |
LIG_MAD2 | 286 | 294 | PF02301 | 0.435 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.496 |
LIG_PCNA_PIPBox_1 | 613 | 622 | PF02747 | 0.622 |
LIG_PCNA_yPIPBox_3 | 613 | 622 | PF02747 | 0.574 |
LIG_PTB_Apo_2 | 351 | 358 | PF02174 | 0.426 |
LIG_Rb_pABgroove_1 | 614 | 622 | PF01858 | 0.521 |
LIG_RPA_C_Fungi | 168 | 180 | PF08784 | 0.463 |
LIG_SH2_PTP2 | 136 | 139 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 624 | 627 | PF00017 | 0.635 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 620 | 624 | PF00017 | 0.596 |
LIG_SH2_STAT3 | 499 | 502 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.610 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.568 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.517 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.447 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.762 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.682 |
LIG_Sin3_3 | 165 | 172 | PF02671 | 0.327 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 164 | 170 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 521 | 528 | PF11976 | 0.378 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.539 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.337 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.484 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.602 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.687 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.557 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.398 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.734 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.600 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.589 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.328 |
MOD_Cter_Amidation | 465 | 468 | PF01082 | 0.335 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.554 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.536 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.339 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.694 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.643 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.413 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.522 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.487 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.409 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.354 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.355 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.596 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.618 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.793 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.600 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.417 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.516 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.621 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.403 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.567 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.409 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.386 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.560 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.619 |
MOD_LATS_1 | 74 | 80 | PF00433 | 0.609 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.403 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.515 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.340 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.415 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.648 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.437 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.445 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.418 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.418 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.693 |
MOD_PIKK_1 | 529 | 535 | PF00454 | 0.567 |
MOD_PIKK_1 | 609 | 615 | PF00454 | 0.627 |
MOD_PK_1 | 245 | 251 | PF00069 | 0.669 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.335 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.560 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.562 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.354 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.398 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.592 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.664 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.600 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.384 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.528 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.434 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.335 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.479 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.504 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.335 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.564 |
MOD_SUMO_rev_2 | 34 | 41 | PF00179 | 0.650 |
MOD_SUMO_rev_2 | 564 | 568 | PF00179 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 550 | 555 | PF01217 | 0.384 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 624 | 627 | PF00928 | 0.635 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 421 | 424 | PF00400 | 0.361 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8D8 | Leptomonas seymouri | 57% | 86% |
A0A1X0P3T2 | Trypanosomatidae | 38% | 100% |
A0A3S5ISG6 | Trypanosoma rangeli | 40% | 100% |
A0A3S7X6Z1 | Leishmania donovani | 92% | 100% |
A4HLV3 | Leishmania braziliensis | 73% | 87% |
D0A670 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AHQ9 | Leishmania infantum | 91% | 86% |
E9B480 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BP75 | Trypanosoma cruzi | 39% | 100% |