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: A0A3Q8IB66
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 | 174 | 178 | PF00656 | 0.758 |
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.687 |
CLV_C14_Caspase3-7 | 538 | 542 | PF00656 | 0.771 |
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.680 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.536 |
CLV_PCSK_PC7_1 | 377 | 383 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.301 |
CLV_Separin_Metazoa | 389 | 393 | PF03568 | 0.710 |
DEG_APCC_DBOX_1 | 376 | 384 | PF00400 | 0.695 |
DEG_APCC_DBOX_1 | 428 | 436 | PF00400 | 0.654 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.722 |
DEG_SPOP_SBC_1 | 88 | 92 | PF00917 | 0.769 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 435 | 444 | PF00134 | 0.669 |
DOC_MAPK_gen_1 | 344 | 352 | PF00069 | 0.740 |
DOC_MAPK_gen_1 | 427 | 435 | PF00069 | 0.662 |
DOC_MAPK_gen_1 | 543 | 552 | PF00069 | 0.723 |
DOC_MAPK_MEF2A_6 | 346 | 354 | PF00069 | 0.703 |
DOC_MIT_MIM_1 | 305 | 313 | PF04212 | 0.743 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.752 |
DOC_PP4_FxxP_1 | 492 | 495 | PF00568 | 0.831 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.838 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.838 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.825 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.756 |
LIG_14-3-3_CanoR_1 | 134 | 142 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 287 | 293 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 381 | 391 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 40 | 47 | PF00244 | 0.775 |
LIG_14-3-3_CanoR_1 | 488 | 492 | PF00244 | 0.822 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 505 | 514 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 579 | 588 | PF00244 | 0.670 |
LIG_APCC_ABBA_1 | 259 | 264 | PF00400 | 0.729 |
LIG_BIR_III_2 | 409 | 413 | PF00653 | 0.653 |
LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.833 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.780 |
LIG_CaM_IQ_9 | 338 | 353 | PF13499 | 0.656 |
LIG_EH_1 | 163 | 167 | PF12763 | 0.668 |
LIG_EVH1_1 | 492 | 496 | PF00568 | 0.837 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.777 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.683 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.752 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.513 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.589 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.689 |
LIG_FHA_2 | 532 | 538 | PF00498 | 0.772 |
LIG_GBD_Chelix_1 | 603 | 611 | PF00786 | 0.510 |
LIG_Integrin_isoDGR_2 | 486 | 488 | PF01839 | 0.472 |
LIG_LIR_Apic_2 | 489 | 495 | PF02991 | 0.833 |
LIG_MYND_1 | 59 | 63 | PF01753 | 0.798 |
LIG_PDZ_Class_3 | 624 | 629 | PF00595 | 0.524 |
LIG_SH2_PTP2 | 595 | 598 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.411 |
LIG_SH3_2 | 60 | 65 | PF14604 | 0.806 |
LIG_SH3_3 | 490 | 496 | PF00018 | 0.820 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.798 |
LIG_SH3_3 | 616 | 622 | PF00018 | 0.571 |
LIG_SUMO_SIM_par_1 | 122 | 128 | PF11976 | 0.826 |
LIG_SUMO_SIM_par_1 | 562 | 569 | PF11976 | 0.652 |
LIG_SUMO_SIM_par_1 | 609 | 616 | PF11976 | 0.682 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.664 |
LIG_TRAF2_1 | 612 | 615 | PF00917 | 0.506 |
LIG_TRAF2_2 | 293 | 298 | PF00917 | 0.798 |
LIG_WRC_WIRS_1 | 130 | 135 | PF05994 | 0.730 |
LIG_WRC_WIRS_1 | 570 | 575 | PF05994 | 0.609 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.777 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.670 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.673 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.675 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.703 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.709 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.633 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.691 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.738 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.541 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.716 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.651 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.670 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.602 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.704 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.624 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.630 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.663 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.744 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.669 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.693 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.700 |
MOD_GlcNHglycan | 537 | 541 | PF01048 | 0.791 |
MOD_GlcNHglycan | 614 | 618 | PF01048 | 0.647 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.758 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.716 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.685 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.751 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.628 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.693 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.563 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.739 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.534 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.598 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.799 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.737 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.615 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.537 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.667 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.641 |
MOD_NEK2_2 | 487 | 492 | PF00069 | 0.691 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.723 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.765 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.669 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.611 |
MOD_PIKK_1 | 579 | 585 | PF00454 | 0.556 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.699 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.724 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.626 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.699 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.675 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.685 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.766 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.735 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.609 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.516 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.614 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.670 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.631 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.752 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.730 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.651 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.691 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.743 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.706 |
MOD_SUMO_rev_2 | 10 | 16 | PF00179 | 0.621 |
MOD_SUMO_rev_2 | 271 | 280 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 450 | 456 | PF00179 | 0.579 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.563 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 543 | 545 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.758 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 381 | 386 | PF00026 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 579 | 583 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCL5 | Leptomonas seymouri | 41% | 94% |
A4HBX1 | Leishmania braziliensis | 73% | 100% |
A4HZ89 | Leishmania infantum | 100% | 100% |
E9AV97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QC83 | Leishmania major | 91% | 99% |