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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 6 |
GO:0016020 | membrane | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0000139 | Golgi membrane | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0031985 | Golgi cisterna | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
Related structures:
AlphaFold database: A4HBX1
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 7 |
GO:0007030 | Golgi organization | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
GO:0000301 | retrograde transport, vesicle recycling within Golgi | 7 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.666 |
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.440 |
CLV_PCSK_PC7_1 | 375 | 381 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.400 |
CLV_Separin_Metazoa | 619 | 623 | PF03568 | 0.396 |
DEG_APCC_DBOX_1 | 374 | 382 | PF00400 | 0.634 |
DEG_APCC_DBOX_1 | 417 | 425 | PF00400 | 0.597 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.640 |
DEG_SPOP_SBC_1 | 102 | 106 | PF00917 | 0.647 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.658 |
DOC_MAPK_gen_1 | 342 | 350 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.596 |
DOC_MAPK_gen_1 | 541 | 550 | PF00069 | 0.665 |
DOC_MAPK_MEF2A_6 | 115 | 124 | PF00069 | 0.630 |
DOC_MAPK_MEF2A_6 | 461 | 470 | PF00069 | 0.540 |
DOC_MIT_MIM_1 | 303 | 312 | PF04212 | 0.637 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.677 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.700 |
DOC_PP2B_LxvP_1 | 618 | 621 | PF13499 | 0.392 |
DOC_PP4_FxxP_1 | 490 | 493 | PF00568 | 0.772 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.639 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 226 | 236 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 38 | 48 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 475 | 480 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 523 | 530 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 559 | 568 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 577 | 586 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 587 | 591 | PF00244 | 0.469 |
LIG_APCC_ABBA_1 | 257 | 262 | PF00400 | 0.624 |
LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.592 |
LIG_BRCT_BRCA1_1 | 486 | 490 | PF00533 | 0.727 |
LIG_EVH1_1 | 490 | 494 | PF00568 | 0.724 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.671 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.719 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.502 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.369 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.652 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.702 |
LIG_LIR_Apic_2 | 487 | 493 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.640 |
LIG_PTB_Apo_2 | 610 | 617 | PF02174 | 0.422 |
LIG_PTB_Phospho_1 | 610 | 616 | PF10480 | 0.417 |
LIG_SH2_NCK_1 | 486 | 490 | PF00017 | 0.624 |
LIG_SH2_PTP2 | 593 | 596 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 486 | 490 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.385 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.752 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.514 |
LIG_SUMO_SIM_par_1 | 120 | 126 | PF11976 | 0.725 |
LIG_SUMO_SIM_par_1 | 607 | 612 | PF11976 | 0.369 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.535 |
LIG_TRAF2_2 | 291 | 296 | PF00917 | 0.700 |
LIG_TRFH_1 | 616 | 620 | PF08558 | 0.386 |
LIG_TYR_ITIM | 454 | 459 | PF00017 | 0.532 |
LIG_UBA3_1 | 8 | 15 | PF00899 | 0.561 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.688 |
LIG_WRPW_2 | 131 | 134 | PF00400 | 0.642 |
LIG_WW_3 | 619 | 623 | PF00397 | 0.396 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.727 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.695 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.678 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.528 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.668 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.630 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.615 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.691 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.567 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.691 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.359 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.498 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.458 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.403 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.475 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.373 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.500 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.531 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.475 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.505 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.447 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.348 |
MOD_GlcNHglycan | 66 | 70 | PF01048 | 0.493 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.594 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.705 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.724 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.658 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.723 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.670 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.531 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.656 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.684 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.609 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.618 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.727 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.613 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.227 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.739 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.686 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.643 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.689 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.679 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.764 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.627 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.633 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.597 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.642 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.638 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.690 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.414 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.674 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.598 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.623 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.689 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.586 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.632 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.414 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.236 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.657 |
MOD_SUMO_rev_2 | 10 | 16 | PF00179 | 0.618 |
MOD_SUMO_rev_2 | 448 | 454 | PF00179 | 0.594 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.609 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.641 |
TRG_NES_CRM1_1 | 458 | 469 | PF08389 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 379 | 384 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 577 | 581 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCL5 | Leptomonas seymouri | 39% | 94% |
A0A3Q8IB66 | Leishmania donovani | 73% | 100% |
A4HZ89 | Leishmania infantum | 73% | 100% |
E9AV97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QC83 | Leishmania major | 72% | 100% |