Structural Proteins, Major sperm
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 6 |
GO:0016020 | membrane | 2 | 6 |
GO:0031090 | organelle membrane | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HXJ8
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022406 | membrane docking | 2 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051643 | endoplasmic reticulum localization | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0061817 | endoplasmic reticulum-plasma membrane tethering | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090158 | endoplasmic reticulum membrane organization | 5 | 1 |
GO:0140056 | organelle localization by membrane tethering | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.538 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.688 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.794 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.689 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.752 |
DOC_CYCLIN_yCln2_LP_2 | 133 | 139 | PF00134 | 0.563 |
DOC_MAPK_gen_1 | 126 | 133 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 38 | 45 | PF00069 | 0.618 |
DOC_MAPK_MEF2A_6 | 86 | 95 | PF00069 | 0.590 |
DOC_PP2B_PxIxI_1 | 40 | 46 | PF00149 | 0.519 |
DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.667 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.590 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.780 |
DOC_USP7_UBL2_3 | 255 | 259 | PF12436 | 0.730 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.729 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 126 | 132 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 298 | 308 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.793 |
LIG_BIR_III_4 | 237 | 241 | PF00653 | 0.673 |
LIG_EH1_1 | 271 | 279 | PF00400 | 0.299 |
LIG_EVH1_2 | 53 | 57 | PF00568 | 0.590 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.721 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.495 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.510 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.590 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.672 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.577 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.586 |
LIG_Integrin_RGD_1 | 155 | 157 | PF01839 | 0.474 |
LIG_LIR_Apic_2 | 181 | 185 | PF02991 | 0.664 |
LIG_LIR_Apic_2 | 321 | 325 | PF02991 | 0.538 |
LIG_LIR_Apic_2 | 393 | 399 | PF02991 | 0.507 |
LIG_LIR_Apic_2 | 423 | 429 | PF02991 | 0.515 |
LIG_LIR_Apic_2 | 449 | 455 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 102 | 111 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 147 | 154 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.695 |
LIG_MYND_1 | 141 | 145 | PF01753 | 0.672 |
LIG_NRBOX | 147 | 153 | PF00104 | 0.609 |
LIG_Pex14_1 | 268 | 272 | PF04695 | 0.366 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.535 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.490 |
LIG_SH2_PTP2 | 187 | 190 | PF00017 | 0.693 |
LIG_SH2_SRC | 187 | 190 | PF00017 | 0.646 |
LIG_SH2_SRC | 375 | 378 | PF00017 | 0.546 |
LIG_SH2_SRC | 447 | 450 | PF00017 | 0.535 |
LIG_SH2_SRC | 452 | 455 | PF00017 | 0.495 |
LIG_SH2_STAT3 | 433 | 436 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.590 |
LIG_SH3_1 | 322 | 328 | PF00018 | 0.530 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.707 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.646 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.560 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.561 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.565 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.503 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.607 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.590 |
LIG_SH3_5 | 429 | 433 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 280 | 286 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 275 | 280 | PF11976 | 0.399 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.483 |
LIG_TRAF2_1 | 382 | 385 | PF00917 | 0.578 |
LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.553 |
LIG_WRC_WIRS_1 | 179 | 184 | PF05994 | 0.663 |
LIG_WW_1 | 184 | 187 | PF00397 | 0.682 |
MOD_CDK_SPK_2 | 141 | 146 | PF00069 | 0.671 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.621 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.758 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.768 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.525 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.545 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.537 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.513 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.782 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.572 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.648 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.564 |
MOD_GlcNHglycan | 225 | 229 | PF01048 | 0.458 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.845 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.400 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.652 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.667 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.826 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.595 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.426 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.555 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.656 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.718 |
MOD_NEK2_2 | 178 | 183 | PF00069 | 0.659 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.638 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.553 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.537 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.592 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.590 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.633 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.809 |
MOD_Plk_2-3 | 135 | 141 | PF00069 | 0.626 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.663 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.697 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.691 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.618 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.732 |
MOD_SUMO_for_1 | 43 | 46 | PF00179 | 0.590 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.693 |
TRG_NLS_Bipartite_1 | 219 | 236 | PF00514 | 0.665 |
TRG_NLS_MonoExtC_3 | 231 | 237 | PF00514 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H717 | Leishmania donovani | 100% | 100% |
A4H978 | Leishmania braziliensis | 65% | 100% |
E9AR93 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QE70 | Leishmania major | 86% | 100% |